The Associate Project Manager supports operational execution by coordinating project activities, stakeholder communications, and financial reporting. They also provide executive support to senior leadership and ensure projects align with established timelines and business objectives.
The role involves coordinating field service staff, scheduling work, and managing equipment setup at various healthcare facilities. You will also provide ongoing customer support, conduct routine product tests, and deliver on-the-job training to new hires.
Drive consultative sales and revenue growth for patient access and support services by identifying client challenges and aligning solutions across pharmaceutical, precommercial, and MedTech accounts. Build executive relationships, develop strategic account plans, win new business, expand existing partnerships, and collaborate with internal teams to deliver strong client experiences.
The Field Service Technician will coordinate field staff, manage equipment setup, and conduct routine product tests after installation. They are also responsible for providing ongoing communication and support to hospital staff while ensuring project needs are met.
The Field Service Technician will coordinate field staff schedules, equipment, and daily operational needs while providing ongoing communication and support to hospital staff. They are also responsible for conducting routine equipment checks, recording test data, and providing on-the-job training for new hires.
Coordinate field service staff schedules, work assignments, tools, and day-to-day needs, and set up equipment and workstations. Conduct routine product checks and record test data, support hospital staff, and provide on-the-job training to new hires.
Coordinate field technicians, schedules, tools, equipment, and on-site work needs. Set up workstations, record product test data, support hospital staff, and train new hires.
The role involves reviewing clinical and safety data to ensure medical accuracy and consistency while supporting study start-up and medical evaluation activities. You will also collaborate with study teams to manage safety deliverables and escalate critical medical cases as necessary.
The Lead Generator will identify and qualify opportunities within a customer portfolio to generate high-quality leads for medical representatives. They are also responsible for scheduling appointments, maintaining professional relationships, and accurately recording interactions in internal systems.
The role involves receiving and documenting incoming safety data, adverse events, and product quality complaints from healthcare providers and patients. The specialist must summarize reports, maintain accurate data entry, and disseminate information according to approved scripts and regulatory guidelines.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory. Additionally, you will build strategic relationships with doctors and pharmacies while implementing creative, digital-first engagement formats.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory by building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable engagement formats that utilize both digital and traditional channels.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory by building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable digital and hybrid engagement formats to interact with healthcare professionals.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory by building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable engagement formats that utilize both digital and traditional channels to interact with healthcare professionals.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory by building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable engagement formats that go beyond traditional face-to-face visits, utilizing digital channels and hybrid interaction models.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory by building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable engagement formats that utilize both digital channels and traditional interactions.
The representative is responsible for receiving and vetting medical claims against program-specific business rules to approve or reject payment assistance. They also provide support to patients and healthcare providers regarding co-pay cards, vouchers, and claim inquiries.
The Therapeutic Strategy Lead develops and implements effective delivery strategies during the RFP/Bid Defense cycle to meet customer needs. They bridge the gap between sales, medical, and operational teams to ensure seamless project execution and drive business growth.
The Therapeutic Strategy Lead develops and implements effective delivery strategies during the RFP/Bid Defense cycle to meet customer needs. They collaborate across sales, medical, and operational teams to ensure project feasibility and drive business growth.
The Care Specialist delivers product and disease-state education to patients while helping them navigate health insurance, access pathways, and affordability resources. They manage an assigned patient caseload through various interaction methods, including in-home and virtual visits, to promote treatment adherence and health literacy.
The Clinical Specialist administers standardized stroke assessments and ensures data quality and consistency throughout clinical trials. They also review assessments conducted by other raters and provide feedback to maintain protocol compliance and inter-rater reliability.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. They are responsible for reviewing assessments conducted by other raters and providing feedback to maintain protocol compliance.
The Associate Medical Safety Director will lead signal detection and analysis while providing medical oversight for safety profiles and aggregate reports. They will also serve as an internal consultant for pharmacovigilance operations and contribute to risk management plans and regulatory submissions.
Review clinical trial case data and rater-administered scales, then conduct live discussions to provide guidance on assessment methods and scoring. Participate in training and calibration, complete scheduled rater interactions, and submit accurate documentation on time.
Design and deliver outcome research studies, including patient-reported outcome and patient-centered research, interviews, and qualitative and quantitative analyses. Support research from concept development through ethics review, client proposals and reports, conference presentations, and publications, while coordinating with clinicians, patients, healthcare sites, and patient groups.
The Senior Recruiter will manage the end-to-end recruitment process for the Clinical Talent Acquisition team in the EMEA region. They will collaborate with business leaders to source, select, and hire qualified candidates while ensuring compliance with company policies and regional hiring guidelines.
The Project Management Analyst supports clinical research projects by monitoring performance metrics, managing timelines, and tracking project financials. They also coordinate team meetings, maintain project documentation, and ensure compliance with quality standards.
The Senior Recruiter will manage the end-to-end recruitment process for the Clinical Talent Acquisition team, including sourcing, interviewing, and hiring qualified candidates. They will also collaborate with business leaders to establish staffing objectives and ensure compliance with regional hiring guidelines.
The Senior Epidemiologist will independently execute real-world evidence initiatives to support early clinical development programs across Phases 1-3. Responsibilities include characterizing disease landscapes, conducting feasibility assessments, and developing study protocols and reports for oncology programs.
The role involves providing medical safety expertise, conducting signal detection, and performing medical evaluations of adverse drug reactions. The director will also contribute to aggregate reports, risk management plans, and provide safety oversight for clinical trials and post-marketing activities.
The Project Manager will lead complex Endoscopy digital implementation projects from intake through closure, ensuring alignment with scope, schedule, and quality standards. They will serve as the primary liaison between internal teams, vendors, and hospital stakeholders to coordinate technical and clinical readiness.
The Epidemiologist will independently execute real-world evidence activities to support inflammation programs across Phase 1-3 clinical development. Responsibilities include conducting feasibility assessments, developing study protocols, and interpreting findings for sponsor stakeholders.
The Contracts Analyst will develop and prepare contracts and budgets for customers while ensuring the scope of work is accurately defined. They will act as the primary interface for small to mid-size projects and manage the contracting process to ensure timely execution.
The Global Trial Manager will lead critical aspects of late-phase clinical trials, ensuring they meet timelines, budgets, and quality standards. They will act as the primary operational point of contact, coordinating activities across global stakeholders and managing regulatory documentation.
The Senior Global Trial Manager will lead critical aspects of global late-phase clinical trials, ensuring they meet timelines, budgets, and quality standards. They will act as the primary operational point of contact, coordinating activities across internal and external stakeholders while maintaining regulatory compliance.
You will manage end-to-end site start-up activities, including site identification, feasibility, and maintenance for clinical trials. Additionally, you will lead budget and contract negotiations while ensuring all documentation complies with regulatory and ethics requirements.
Care Managers handle outbound and inbound calls to insurance companies and patients to manage benefit investigations, prior authorizations, and copay assistance programs. They are responsible for documenting information accurately while maintaining HIPAA compliance and meeting program quality standards.
The Clinical Trial Safety Scientist is responsible for the ongoing review of patient-level clinical and safety data to ensure medical accuracy and consistency. They also facilitate safety data meetings, contribute to study start-up activities, and escalate critical medical cases to study physicians.
The Business Process Analyst will analyze financial contracts, validate data, and resolve chargeback claims to ensure accuracy and efficiency. They will also manage multiple accounts, track work progress, and provide support to team members to meet organizational objectives.
The role involves drafting, reviewing, and negotiating clinical, vendor, and non-disclosure agreements while ensuring compliance with legal and organizational policies. The analyst will also coordinate contract processes, track metrics, and support negotiations through direct communication with customers and vendors.
The Site Activation Coordinator manages feasibility, site identification, and regulatory start-up activities for clinical trials. They serve as the primary point of contact for investigative sites, ensuring all documentation and contracts are accurately prepared and executed.
The Contract Negotiation Specialist is responsible for independently drafting, reviewing, and negotiating clinical trial agreements with investigative sites. They manage contract portfolios to ensure study timelines are met while maintaining compliance with regulatory and sponsor requirements.
The analyst will review scientific literature to extract and maintain psychometric data within the COAA platform. They are responsible for performing quality control checks to ensure the accuracy, consistency, and completeness of clinical outcome assessment records.
Engage with healthcare customers and translate their needs and market insights into initiatives to develop products, services, and solutions, while identifying new business opportunities. Manage internal business development projects and stakeholder relationships, prepare customer and management briefings, and contribute to public tenders.
Monitor Phase I–IV oncology clinical trials and manage site activities from start-up through close-out, ensuring compliance with study protocols, GCP/ICH guidelines, and regulatory requirements. Train site personnel, oversee documentation and investigational product accountability, resolve data queries, maintain site communications, and prepare monitoring reports.
Review, assess, and process safety data, and submit and distribute safety reports to regulatory authorities and other parties in accordance with regulations, SOPs, and project requirements. Track cases, identify quality issues, collaborate with internal teams and healthcare professionals, and provide project feedback to the operations manager.
The recruiter will source, select, and hire qualified candidates while collaborating with management to meet staffing objectives. They are also responsible for writing job advertisements, conducting interviews, and utilizing market intelligence to drive recruitment strategies.
The Associate Project Manager will plan, execute, and close small to medium-sized connected device projects within clinical studies while ensuring they meet sponsor requirements. They are responsible for coordinating cross-functional teams, managing project risks, and maintaining project documentation and databases.
The Associate Project Manager will oversee small to medium-sized connected device projects across all clinical study phases, ensuring they meet sponsor requirements within budget and timelines. Responsibilities include coordinating cross-functional teams, managing project risks, and maintaining internal databases while providing regular updates to stakeholders.
The Associate Data Scientist will assist with client engagements by measuring data de-identification and re-identification risks. Responsibilities include preparing client datasets, validating data, and supporting the delivery of privacy solutions through reports and remote coaching.
The Data Analyst will perform data analytics activities to provide insights for business problems and support internal project teams. Responsibilities include updating and maintaining databases, monitoring data trends, and identifying anomalies in projected data.
You will recruit and engage healthcare professionals to participate in market research studies by building trustful relationships. This involves conducting outbound calls, managing follow-ups, and maintaining accurate records of participant status.
You will independently manage a network of pharmacies, conducting on-site training sessions for pharmacy staff regarding OTC products and medications. Additionally, you are responsible for planning your own routes and appointments while supporting pharmacy partners with promotional campaigns.
The Local Clinical Study Manager provides operational and scientific oversight for clinical trials, ensuring quality, timelines, and regulatory compliance. They lead cross-functional teams, manage site startup activities, and coordinate with vendors to achieve study objectives.
The Project Management Analyst supports clinical project leaders by managing project schedules, finances, and risk mitigation strategies. They are responsible for maintaining performance dashboards, ensuring data accuracy, and facilitating effective communication between internal teams and customers.
The Senior Medical Director provides strategic medical and scientific expertise to support clinical research and development lifecycle activities. They lead proposal development, participate in client bid defense meetings, and oversee the execution of therapeutic group strategies.
Coordinate country-level site activation and start-up activities, serving as the point of contact for investigative sites and internal project teams. Prepare, review, track, and quality-check regulatory and contractual documents while maintaining project systems, timelines, and site performance information.
Coordinate clinical laboratory study activities from start-up through close-out, including documentation, site operations, shipments, monitoring, and issue escalation. Collaborate with internal teams and external stakeholders, communicate with customers when the Project Manager is unavailable, and support audits, inspections, and training.
Lead and manage the strategic, operational, and financial delivery of global site activation activities across assigned studies. Oversee regulatory submissions, site contracting, and project timelines while collaborating with internal and external stakeholders to ensure efficient study start-up.
The Sales Support Analyst is responsible for maintaining CRM data integrity and supporting sales operations including quoting, contracting, and order processing. They will also validate account information and resolve data discrepancies to ensure accurate reporting and compliance.
The Principal Biostatistician provides statistical analysis support for Phase 2 and 3 clinical trials and authors statistical analysis plans. They also collaborate with multi-disciplinary teams to interpret study results and provide guidance to programmers.
The Therapeutic Strategy Lead develops and implements effective delivery strategies during the RFP and bid defense cycle to meet customer needs. They bridge the gap between sales, medical, and operational teams to ensure seamless project execution and business growth.
The Therapeutic Strategy Lead develops and implements effective delivery strategies during the RFP and bid defense cycles to support business growth. They collaborate across sales, medical, and operational teams to ensure project strategies are feasible and aligned with customer needs.
The consultant will perform active outreach to healthcare professionals and establishments to promote and sell products via phone and digital channels. They are responsible for managing the sales cycle, maintaining CRM records, and ensuring sales targets are met.
The Data Analyst will perform quantitative and qualitative analyses to provide insights for business problems and support project teams. They are responsible for identifying data trends, creating reports, and ensuring data accuracy using existing tools.
The Medical Strategy Lead provides strategic medical and scientific expertise to support clinical development plans and proposal development within the hematology-oncology therapeutic area. They act as an internal and external consultant throughout the research and development lifecycle, guiding project teams and engaging with clients to ensure scientific and regulatory soundness.
The Senior Medical Director provides strategic medical and scientific expertise to support clinical research and development lifecycle activities. They lead proposal development, participate in client bid defense meetings, and oversee the execution of therapeutic group strategies.
The Medical Strategy Lead provides strategic medical and scientific expertise to support clinical development plans and proposal development within the Hematology-Oncology Center of Excellence. They act as an internal and external consultant throughout the research and development lifecycle, guiding project teams and sponsors on clinical strategy and protocol design.
The Medical Strategy Lead provides scientific and clinical expertise to support proposal development, protocol design, and clinical trial execution within the Hematology-Oncology Center of Excellence. They act as an internal and external consultant, guiding project teams and sponsors throughout the research and development lifecycle.
The Medical Director provides strategic scientific leadership across client accounts and leads, mentors, and develops a team of scientific professionals. They are responsible for ensuring the quality and integrity of client deliverables while driving business growth and operational excellence.
Perform site activation, feasibility, and maintenance activities for investigative sites in accordance with regulations and SOPs. Manage and track essential study documents while collaborating with project management and site activation teams.
The specialist will serve as the primary point of contact for investigative sites and project teams to coordinate site activation and regulatory activities. They are responsible for preparing regulatory documentation, managing contract negotiations, and ensuring compliance with local regulations and project timelines.
The Study Start Up Specialist manages site activation activities and serves as the primary point of contact for investigative sites and project teams. They ensure all regulatory documents are accurate, compliant with SOPs, and completed within project timelines.
The Medical Data Review Manager is responsible for reviewing structured clinical patient data to ensure medical plausibility, protocol adherence, and data completeness. They also collaborate with clinical sites and internal teams to investigate anomalies and verify patient information readiness for further review.
The Centralized Monitoring Analyst is responsible for setting up, programming, and refreshing the Centralized Monitoring platform to support study-specific quality and risk indicators. They work directly with clients to manage deliverables and ensure data quality through ongoing monitoring and assessment.
Develop, test, and validate clinical data programs while ensuring compliance with CDISC SDTM standards. Collaborate with cross-functional teams to provide data visualization and technical mentorship to junior staff.
The Licensing Manager leads the end-to-end execution of COA and eCOA licensing services for global clinical studies while acting as a subject matter expert for clients. They are responsible for managing delivery teams, ensuring operational excellence, and supporting commercial growth through proposal development and client expansion.
The specialist will process and submit safety reports to regulatory authorities while ensuring compliance with SOPs and project requirements. They will also liaise with functional team members and healthcare professionals to address project-related issues and provide feedback on operational performance.
The Medical Data Review Manager will review structured clinical patient data to ensure medical plausibility and protocol adherence. They will also identify data anomalies and collaborate with clinical sites to maintain the accuracy and readiness of patient information for review.
The Senior Medical Director provides strategic medical and scientific expertise to lead clinical development plans and group strategy within the Obesity therapeutic area. They are responsible for driving proposal development, leading bid defense meetings, and acting as a consultant throughout the research and development lifecycle.
The Senior Medical Director provides strategic medical and scientific expertise to lead clinical development plans and therapeutic area strategies. They act as a consultant throughout the research and development lifecycle and lead client proposal bid defense meetings.
The Principal Biostatistician provides comprehensive statistical support for drug development based on real-world evidence. They serve as the statistical lead for health outcomes and epidemiology studies while collaborating with multidisciplinary teams.
The role involves administering psychiatric assessments to clinical trial participants and evaluating the quality of assessments performed by other raters. You will ensure data reliability through standardized methodology and provide feedback on scoring techniques.
The role involves programming, validating, and delivering high-quality NONMEM-ready PK/PD datasets while ensuring compliance with SDTM/ADaM standards. The programmer will also conduct quality control of datasets and collaborate with cross-functional teams to resolve data issues and support regulatory submissions.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while overseeing data reconciliation, budgets, and cross-functional team performance.
The Community Medical Liaison provides disease awareness and product education to multidisciplinary treatment teams, patients, and caregivers. They also gather clinical insights and collaborate with advocacy organizations to address educational gaps in the neuroscience therapeutic area.
The Principal Biostatistician collaborates with multi-disciplinary teams to design clinical trials, perform sample size calculations, and author statistical analysis plans. They also provide statistical expertise for regulatory submissions and oversee the validation of analysis datasets and reporting outputs.
The Principal Biostatistician provides comprehensive statistical support for drug development projects focused on real-world evidence. They serve as the statistical lead for health outcomes and epidemiology studies while collaborating with multi-disciplinary teams to develop study protocols and analysis plans.
The Principal Biostatistician provides statistical support for clinical trials, including study design, sample size calculations, and authoring statistical analysis plans. They also collaborate with cross-functional teams to ensure accurate reporting and regulatory compliance for clinical study documents.
The Product Owner is responsible for the professional development of the product, including translating business requirements into user stories and maintaining the product backlog. They act as the primary interface between stakeholders, development teams, and users to ensure product quality and alignment with strategic goals.
The specialist will coordinate country-specific site activation and regulatory activities while serving as the primary point of contact for investigative sites and project teams. They are responsible for managing regulatory documentation, contract negotiations, and ensuring compliance with local regulations and project timelines.
The Therapeutic Strategy Director leads the design of innovative clinical development strategies for sponsors from First-in-Human through Phase IIa studies. They are responsible for driving business growth by leading cross-functional teams in proposal development and maintaining high-level client relationships.
The Site Activation Specialist acts as the primary point of contact for clinical study start-up activities, ensuring compliance with local regulations and project timelines. They are responsible for managing site documentation, performing feasibility assessments, and coordinating with internal teams to ensure successful site activation.
The Associate Medical Director provides strategic scientific leadership across client accounts and leads, mentors, and develops a team of medical and scientific professionals. They serve as a senior advisor to clients, ensuring the quality and integrity of deliverables while driving business growth and operational excellence.
Lead client workshops and discovery sessions to analyze business needs and recommend industry best practices for CRM and Speaker Bureau implementations. Partner with cross-functional teams to translate business requirements into functional specifications and support the full deployment lifecycle.
The Medical Director acts as a global or regional medical advisor, providing support for clinical protocols, patient safety, and eligibility determinations. They also perform medical reviews of adverse events, serious adverse events, and clinical study reports in collaboration with the pharmacovigilance department.
The Site Payments Analyst ensures accurate and timely payments to clinical trial sites by managing fee schedules, validating invoices, and coordinating with contract managers. They also act as the primary point of contact for sites regarding payment processes and support financial reporting throughout the study lifecycle.
The representative will process medical claims by reviewing documentation and vetting them against program-specific business rules. They will also provide payment assistance solutions and support customer inquiries via various communication channels.
The Principal Statistical Programmer ensures the accuracy and integrity of clinical trial data by developing and validating complex datasets using SAS and R. They also provide technical guidance, mentor junior staff, and collaborate with cross-functional teams to optimize programming workflows.
The Regulatory and Start Up Specialist serves as the single point of contact for investigative sites and project teams to manage site activation activities. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and tracking project timelines to ensure successful site initiation.
The Associate Medical Director provides medical support for clinical trials, including protocol clarifications, patient safety monitoring, and adverse event reviews. They also collaborate with the Pharmacovigilance department and provide therapeutic area training to project teams.
The Creative Operations Lead will oversee a global team of designers, manage studio workflows, and ensure the quality and accuracy of production-ready mechanicals. They will partner with cross-functional teams to forecast workloads, resolve bottlenecks, and maintain brand integrity across all deliverables.
The CRA is responsible for performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with regulatory requirements. They also manage study progress by tracking regulatory submissions, recruitment plans, and data integrity.
Conduct virtual consultations and sales discussions to educate dental professionals on oral care products. Build and maintain strong customer relationships while achieving performance and engagement targets.
The VP & Managing Director will serve as the senior operational liaison for mid-sized pharmaceutical customers, leading strategic partnerships and mobilizing global teams to ensure high-quality delivery. They are responsible for driving organic growth, managing portfolio-level risks, and achieving annual net revenue targets of $100M+.
Perform site monitoring, management, and start-up activities for Real World Evidence studies while ensuring compliance with protocols and regulations. Coordinate regulatory submissions, site activation, and ongoing communication to drive study timelines and data integrity.
The Site Activation Specialist manages site feasibility, regulatory documentation, and contract negotiations for clinical research projects. They serve as the primary point of contact for investigative sites and ensure all project timelines and SOP requirements are met.
Translate written materials from English into Korean while preserving the original meaning, structure, and style, and proofread translations for terminology, grammar, spelling, and punctuation. Collaborate with the translation team to maintain and improve glossaries, translation memories, and style guides, identify instruction or project risks, and deliver accurate work on time.
Conduct structured and semi-structured interviews with clinical trial participants with Borderline Personality Disorder, administering, scoring, and documenting validated rating scales. Maintain inter-rater reliability and protocol compliance, escalate safety concerns, and collaborate with investigators, site staff, and sponsor or CRO teams.
Perform interim monitoring visits at clinical trial sites to ensure protocol adherence and ICH-GCP compliance. Collaborate with project teams to verify study data and manage site action plans.
The Business Development Director will prospect, qualify, and close new sales opportunities for data and technology solutions within the healthcare payer market. They are responsible for driving strategic account growth, managing the full sales cycle, and consistently meeting or exceeding assigned revenue targets.
The Global Key Account Director will lead strategic relationships with pharmaceutical clients to drive revenue growth and deliver integrated solutions. They are responsible for orchestrating cross-functional teams and managing the full client lifecycle to ensure long-term partnership success.
The RSU Specialist serves as the single point of contact for investigative sites and project teams to manage study start-up and maintenance activities. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and maintaining accurate project tracking systems.
Conduct independent, standardized psychiatric assessments of patients for a major depressive disorder clinical study. Administer, score, review, or oversee MADRS and MINI assessments to support the quality and integrity of clinical trial outcomes.
The Clinical Independent Rater reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also conduct patient interviews and administer clinical rating scales while ensuring protocol compliance and data integrity.
Care Managers handle insurance eligibility, benefit investigations, and prior authorizations while providing support to patients and providers. They also manage inbound and outbound calls to assist with pharmacy services and copay assistance programs.
The role involves providing centralized global clinical trial oversight within an FSP model, managing study teams, and ensuring high standards of quality and inspection readiness. You will also oversee CROs and global vendors while driving trial delivery from start-up through close-out.
The Senior Director provides strategic and operational leadership for Clinical Pharmacology, Biostatistics, and Statistical Programming functions. They are responsible for overseeing study design, regulatory submissions, resource planning, and driving innovation across clinical development programs.
You will be responsible for achieving sales and market share targets for vaccines within your assigned territory while building strategic relationships with doctors and pharmacies. Additionally, you will develop and implement creative, scalable engagement formats that go beyond traditional face-to-face visits, including digital and hybrid interaction models.
Direct and manage the strategic, operational, and financial execution of site activation activities, including site selection, regulatory processes, and contract negotiations. Collaborate with internal and external stakeholders to ensure project timelines and quality standards are met across multiple regions.
Perform site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation. Manage study progress by tracking regulatory submissions, recruitment plans, and data query resolutions.
The representative serves as the primary contact for patients and medical professionals, handling requests such as card activation, program eligibility, and benefit explanations. They are responsible for assessing user issues, providing first-level support, and documenting resolutions while escalating complex problems.
The specialist will process, assess, and submit safety reports to regulatory authorities in compliance with SOPs and project requirements. They will also liaise with functional team members and healthcare professionals to address project-related issues and report quality findings to senior staff.
Oversee end-to-end data management delivery for global clinical trials, including study setup and database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
The Nurse Educator delivers remote and in-person patient education, including medication administration training and adherence support. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections to program-approved resources.
The Commercialization Partner acts as a trusted advisor to emerging biopharma clients, developing integrated commercialization strategies and launch plans. They are responsible for managing client engagements, identifying new business opportunities, and mentoring team members to deliver high-quality solutions.
The consultant will provide high-quality consulting support for MedTech projects by conducting primary market research and quantitative analysis. They will also develop strategic recommendations and create compelling client-facing presentations to help clients make informed business decisions.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining project documentation and ensuring compliance with industry standards and regulations.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining project documentation and ensuring compliance with industry standards and regulations.
The coordinator will perform site activation, feasibility, and maintenance activities for investigative sites in accordance with regulations and SOPs. They are responsible for preparing, reviewing, and distributing site documents while maintaining internal systems and tracking project timelines.
The Clinical Independent Rater reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also participate in training and calibration activities while ensuring accurate documentation of clinical trial data.
Maintain and drive growth for priority accounts by maximizing opportunities through successful negotiation. Collaborate with internal and external stakeholders to defend and expand specific pharmaceutical accounts.
The Medical Director serves as a medical monitor for clinical trials, providing scientific expertise and oversight for rheumatologic research. They support investigative sites with protocol-related issues, manage adverse events, and contribute to medical strategy for client proposals.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation. Additionally, the CRA will manage study progress by tracking regulatory submissions, recruitment plans, and data integrity.
The Data Team Lead manages end-to-end data management services for clinical projects, ensuring quality deliverables are met within budget and timelines. They provide leadership to the team, oversee data cleaning activities, and facilitate communication between stakeholders and the programming team.
Conduct remote dermatology consultations via telephone or video to assess, diagnose, and manage common skin conditions. Develop and implement tailored treatment plans while maintaining accurate clinical records in accordance with professional standards.
The Nurse Educator delivers remote and in-person patient education regarding medication administration and treatment adherence. They also collaborate with healthcare providers and field leadership to ensure program compliance and optimal patient outcomes.
This role involves leading complex, client-facing revenue management and system integration engagements while managing and developing a team of functional and technical resources. The principal will own end-to-end implementations and provide subject matter expertise across the pharmaceutical revenue management ecosystem.
The Associate Medical Director provides medical, clinical, and scientific advisory expertise for assigned clinical trials and business development activities. Responsibilities include medical monitoring, protocol review, and providing strategic guidance to internal stakeholders and investigative sites.
The TMF Quality Project Manager serves as a liaison between Records Management and user departments to ensure clinical research records are maintained according to SOPs and regulatory requirements. They oversee the transfer, imaging, and disposition of project records while providing functional leadership to project teams.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while overseeing data reconciliation, timelines, and budgets.
The specialist manages site activation activities, including feasibility assessments, regulatory documentation, and site identification. They also negotiate contracts and budgets while serving as the primary point of contact for investigative sites.
The analyst will evaluate and support the development of AI-enabled healthcare analytics solutions to improve provider performance insights. They will collaborate with cross-functional teams to translate business requirements into effective analytical capabilities and validate AI-generated outputs.
The Project Lead manages the delivery of Site Enablement Solutions by coordinating planning, implementation, and operational strategies across global clinical trials. They act as internal consultants to study teams and sponsors, ensuring projects meet financial performance goals and quality standards.
Perform site selection, initiation, monitoring, and close-out visits to ensure study compliance with protocols and regulations. Manage site progress by tracking regulatory submissions, recruitment, and data query resolution.
The Contract Negotiator will support start-up contracting activities, including developing grant estimates and managing contract templates for clinical trials. They will collaborate with sponsors and internal stakeholders to ensure compliance with regulatory requirements and project timelines.
The specialist serves as the single point of contact for investigative sites and project teams to manage site activation activities and regulatory documentation. They are responsible for ensuring adherence to SOPs, maintaining project timelines, and performing quality control on site-related documents.
The Site Activation Specialist manages feasibility, site identification, regulatory start-up, and maintenance activities for clinical trials. They serve as the primary point of contact for investigative sites and ensure all documentation and contracts are executed according to project timelines.
Direct and manage the strategic, operational, and financial execution of site activation activities, including site selection, regulatory processes, and contract negotiations. Collaborate with internal and external stakeholders to ensure project timelines and quality standards are met throughout the clinical study lifecycle.
The Clinical Research Associate II participates in the preparation and execution of Phase I-IV clinical trials while overseeing site evaluation, initiation, and monitoring activities. They ensure compliance with Good Clinical Practices and maintain data integrity through source verification and site correspondence.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Oversee regulatory submissions, site contracting, and project timelines to ensure efficient study start-up and patient enrollment.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Collaborate with internal and external stakeholders to ensure efficient study start-up, regulatory compliance, and timely patient enrollment.
The supervisor will coordinate and develop virtual medical visit teams to ensure commercial objectives and quality standards are met. They are responsible for managing remote talent, analyzing performance data, and strengthening relationships with healthcare clients.
The role involves administering, scoring, and reviewing psychiatric assessments such as MINI and MADRS for a depression study. You will act as a Central Independent Rater to support clinical trial data integrity.
The role involves managing and coding medical data collected from healthcare settings to support pharmaceutical research and market analysis. Responsibilities include data entry, quality control, data cleansing, and mapping to ensure high-quality information for clinical development.
The Practice Lead will oversee a specialized medical and scientific communications business, focusing on driving growth, client retention, and operational excellence. They will lead cross-functional teams to deliver integrated, technology-enabled solutions while fostering a collaborative and high-performing culture.
You will perform site selection, initiation, monitoring, and close-out visits while ensuring adherence to Good Clinical Practice and study protocols. Additionally, you will manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
The Senior Clinical Research Associate is responsible for site management and monitoring activities across the country for a single sponsor. They will drive subject recruitment plans, provide protocol training, and maintain monitoring visit reports.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments to maintain high-quality clinical research outcomes.
The role involves driving sales and account management activities within the European biotech sector to expand the client base. Responsibilities include developing robust account strategies and managing high-level relationships with C-suite executives to sell integrated clinical solutions.
The Data Acquisition Specialist is responsible for defining, setting up, and ingesting external data streams in alignment with clinical trial protocols. They liaise with stakeholders and external providers to ensure data accuracy, compliance, and timely transfer for clinical monitoring and analysis.
Manage contract strategy and oversee start-up contracting activities for complex clinical studies and multi-protocol programs. Collaborate with sponsors and internal teams to ensure operational excellence, compliance, and the delivery of high-quality site agreements.
The Senior Site Contracts Associate manages contract strategy and oversees all start-up contracting activities for complex clinical studies. They also collaborate with sponsors and internal teams to ensure operational excellence, compliance, and accurate financial reporting.
Manage contract strategy and oversee all start-up contracting activities for complex clinical studies and multi-protocol programs. Collaborate with sponsors and internal teams to ensure high-quality delivery, compliance, and efficient study initiation.
The Clinical Research Associate is responsible for performing site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation. They also manage study progress by tracking regulatory submissions, recruitment plans, and data integrity.
The Senior Site Contracts Associate will manage contract strategy and oversee all start-up contracting activities for complex clinical studies. They will also collaborate with sponsors and regional teams to ensure operational excellence, compliance, and accurate financial reporting.
The Central Independent Rater will administer, score, and review psychiatric assessments for a depression study. You will work as part of a global team to support clinical trial data integrity and patient outcomes.
The Senior Director will lead global sales strategy and build strategic partnerships within the Emerging Biopharma portfolio to drive revenue growth. They will orchestrate cross-functional teams to deliver integrated solutions that address customer development and commercialization priorities.
Perform site monitoring visits to ensure compliance with regulatory requirements and Good Clinical Practice guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data integrity across assigned clinical sites.
The Clinical Research Associate II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. They manage site activities from start-up through close-out, including site visits, training, and documentation quality assurance.
The Medical Science Liaison will drive pre-launch medical readiness for HDV by mapping key centers and building credible peer-to-peer scientific relationships with healthcare professionals. Additionally, the role involves gathering actionable field insights and providing secondary support for clinical trial execution.
The Product Manager will manage and prioritize product enhancements for the Capitation Adjudication platform while collaborating with cross-functional teams to define requirements. They will also support implementation, testing, and release activities to ensure the platform meets client and business needs.
The Clinical Independent Rater ensures the integrity of clinical trial data by reviewing assessment quality and providing guidance to raters. Responsibilities include conducting live interactions with raters to provide feedback on methodology and scoring techniques.
The Virtual Patient Educator provides education and resources to patients regarding diabetes treatments and prescribed medications. They conduct one-on-one communications with patients via telephone, video, email, and SMS while maintaining accurate documentation.
The role involves overseeing end-to-end SDTM activities, including CRF design management and ensuring vendor specifications comply with CDISC standards. You will collaborate with sponsor colleagues and CRO partners to plan data receipt and ensure the quality and completeness of SDTM datasets.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also conduct live interactions with raters to provide guidance on methodology, scoring techniques, and performance support.
The Project Manager will act as the primary point of contact for eCOA studies, managing project scope, timelines, and budgets. They are responsible for leading client meetings, overseeing system changes, and ensuring compliance with operational standards.
The Clinical Specialist administers standardized stroke assessments and ensures data quality for clinical trials. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring methodology.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. You will provide feedback on methodology and scoring while maintaining accurate documentation for all assigned tasks.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. The consultant will also provide feedback on methodology and scoring while maintaining accurate documentation for all assigned tasks.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment quality to ensure standardized practices. They provide guidance to raters through live discussions and support performance through functional assessments.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments like mock interviews.
The role involves programming, validating, and delivering NONMEM-ready PK/PD datasets while ensuring compliance with SDTM/ADaM standards. The candidate will collaborate with cross-functional teams to resolve data issues and support regulatory submissions through high-quality dataset creation.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to empower patients in their treatment journey. They also maintain accurate documentation, collaborate with field leadership, and ensure compliance with program protocols and regulatory standards.
The Senior CRA is responsible for performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. They also manage study progress by tracking regulatory submissions, recruitment, and data integrity.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to improve treatment outcomes. They also facilitate connections to program-approved resources and maintain accurate documentation while collaborating with field leadership.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence while maintaining accurate documentation and compliance standards. They facilitate connections to program-approved resources and collaborate with field leadership to support patients throughout their treatment journey.
The Nurse Educator provides remote and in-person patient education regarding medication administration and disease management to improve treatment adherence. They also collaborate with healthcare providers and field leadership to maintain program standards and support patients throughout their treatment journey.
Perform complex rebate calculations for managed care, Medicaid, and government programs while ensuring SLA compliance. Analyze utilization data to create accurate client deliverables and collaborate with onshore US teams.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor companies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
The Clinical Specialist reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also participate in calibration activities and ensure the integrity of clinical trial data through live interactions and documentation.
The Clinical Trial Nurse conducts in-home visits to perform study-related procedures, collect biological samples, and document clinical data. They ensure patient safety and protocol compliance while communicating effectively with study teams.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance solutions and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections via phone, email, or fax.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include card activation, verifying program eligibility, and troubleshooting submission rejections.
The Pharmacy Support Call Center Representative provides payment assistance solutions and fields requests regarding card activation, program eligibility, and benefit explanations. They are responsible for documenting information, resolving issues, and escalating complex cases to the appropriate department.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections.
The Nurse Educator provides remote and in-field patient education regarding medication administration and treatment adherence to empower patients in managing their disease. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and approved healthcare resources.
The Nurse Educator provides remote and in-field patient education regarding medication administration and treatment adherence to improve health outcomes. They also facilitate communication between patients and healthcare providers while maintaining accurate documentation and compliance with program protocols.
The Flex Nurse Educator provides remote and occasional in-field educational support and medication training to patients with chronic diseases. They facilitate connections to resources, maintain accurate documentation, and collaborate with leadership to ensure program compliance and patient adherence.
The Regulatory and Start Up Specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. They are responsible for preparing and reviewing regulatory documents, maintaining internal databases, and coordinating with investigative sites and project teams.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and functional assessments.
The representative is responsible for receiving and reviewing medical claims against program-specific business rules to determine approval or rejection. They also provide payment assistance solutions and support customer inquiries via various communication channels.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring techniques.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring methodology.
The role involves managing client relationships and project delivery for connected devices within clinical research. Responsibilities include developing departmental strategy, overseeing quality control, and ensuring compliance with regulatory guidelines.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections.
The Therapeutic Strategy Director leads cross-functional teams to design innovative, client-centric solutions for internal medicine programs during the proposal and business development phase. They are responsible for securing new business, managing high-level client relationships, and ensuring the successful translation of strategy into operational delivery.
The Associate Director is responsible for driving business growth through a consultative sales approach across pharmaceutical and MedTech accounts. They will identify new opportunities and manage relationships to provide integrated solutions for patient access, affordability, and adherence.
Perform monitoring and site management to ensure clinical studies adhere to protocols, regulations, and sponsor requirements. Manage site practices, including recruitment planning, regulatory submissions, and data integrity.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data standardization. You will provide feedback on scoring techniques, manage documentation, and conduct remote interactions with participants and raters.
Deliver high-quality diabetic care and education to patients across various settings, including remote consultations. Collaborate with multidisciplinary teams to support holistic patient care and participate in health initiatives.
The representative will serve as the primary contact for patients and medical professionals to assist with program eligibility, card activation, and benefit explanations. They are responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and the accurate scoring of study-specific rating scales.
Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and consistency while administering specific rating scales.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include conducting live interactions to improve scoring techniques and supporting rater performance through functional assessments.
Lead the implementation of evidence synthesis projects to support HTA and regulatory submissions from pre-award to final delivery. Manage project teams, oversee financial and administrative requirements, and drive business development through proposals and bid defenses.
Drive new and expansion revenue for digital marketing offerings targeting hospital and health system clients across the West Coast. Partner with Account Directors to identify growth opportunities and deliver data-driven solutions that improve service line performance.
Lead complex enterprise client implementations from kickoff through deployment, serving as a trusted advisor to senior stakeholders. Coordinate with cross-functional teams to translate business requirements into technical specifications and ensure successful project execution.
The role involves performing site selection, initiation, monitoring, and close-out visits for a specific pharma client. Responsibilities include managing regulatory submissions, tracking recruitment, and ensuring the quality and integrity of site practices.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
Lead the implementation of evidence synthesis projects to support HTA and regulatory submissions from pre-award to final delivery. Manage project teams, oversee operational and financial requirements, and drive business development through proposal creation and lead qualification.
Lead the design and implementation of methodologically rigorous evidence synthesis and HTA-compliant studies. Manage project delivery, oversee junior staff, and develop analyses using R to support client business objectives.
Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.
Manage start-up contracting activities, including developing investigator grant estimates and maintaining contract templates for biotech sponsors. Ensure compliance with regulatory requirements and project timelines while collaborating with stakeholders and RSU regions.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Act as the primary client contact while managing budgets, timelines, and mentoring junior staff.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
Provide scientific and strategic epidemiology support for clinical development and drug safety activities within the Inflammation RWE team. Design and conduct observational research studies using real-world data to inform regulatory and clinical decisions.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining essential trial documentation.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining essential trial documentation.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Develop and implement corporate architecture and strategies in collaboration with international teams and management. Analyze existing systems to create innovative software solutions while ensuring compliance with regulatory requirements and engineering standards.
Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and clinical development plans. Act as a subject matter expert and consultant throughout the research and development lifecycle to guide project teams and sponsors.
The role involves managing clinical trial start-up activities, including EU-CTR compilation and regulatory submissions for investigative sites in Belgium. The specialist will act as the primary contact for sites, ensuring compliance with ICH-GCP and project timelines.
Manage start-up contracting activities, including developing investigator grant estimates and proposal text for biotech sponsors. Ensure compliance with regulatory requirements and maintain internal tracking systems like CTMS to meet project timelines.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory, ethics, and contractual documents are accurately prepared and executed according to project timelines.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining essential documentation. Responsibilities also include managing subject recruitment, tracking regulatory submissions, and ensuring the quality and integrity of site practices.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining essential documentation. Responsibilities also include managing subject recruitment, tracking regulatory submissions, and ensuring the quality and integrity of site practices.
The Clinical Specialist reviews psychiatric scales and provides guidance to raters on methodology and scoring techniques. They ensure the integrity of clinical trial data through functional assessments and mock interviews.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
Perform strategic qualitative and quantitative analyses to derive actionable insights for pharmaceutical and healthcare clients. Collaborate with project managers and business intelligence units to create reports, presentations, and project deliverables.
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Monitor patient progress and adherence while maintaining accurate clinical documentation for clinical research studies.
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients in clinical trials. Provide ongoing dietary counseling and monitor patient progress while maintaining accurate clinical documentation.
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
The Senior CRA is responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. They conduct site visits, support subject recruitment, and maintain essential study documentation to ensure data integrity.
The nurse will provide direct support in nursing consultations and coordinate patient care with other specialized services like psychology and nutrition. This role focuses on improving patient quality of life, functional autonomy, and therapeutic adherence within a patient support program.
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
The Medical Writer will be responsible for creating clinical trial-related documents such as protocols, clinical study reports, and CTD modules, as well as authoring post-marketing surveillance documents and clinical study reports/papers. They will also perform Quality Control (QC) checks on various documents.
The Lead Medical Writer will be responsible for creating and reviewing clinical trial documents such as protocols, CSRs, and CTDs, as well as adapting global protocols for Japanese requirements. Responsibilities also include managing projects, resources, budgets, client interactions, and mentoring junior staff.
Remote Registered Dieticians are responsible for conducting nutritional assessments and developing personalized dietetic plans for clients with various disease classifications via telecommunications. They must also provide ongoing dietetic counseling and support to clients and their families while maintaining accurate and confidential client records.
The Call Center Agent will conduct inbound and outbound calls to notify potentially affected facilities and maintain a high level of professionalism and confidentiality. They will also manage data entry and perform general clerical duties.
The Project Manager III will write requirements for assigned IRT studies and manage their implementation to ensure patients receive the correct study drug according to the Sponsor’s protocol. This role involves consulting with clients, managing timelines, and overseeing user acceptance testing.
The Site Payments Analyst ensures accurate and timely payments to clinical trial sites by monitoring payable items and validating invoices against completed services. They also participate in trial oversight meetings and coordinate with contract managers to maintain accurate payment terms.
Lead and coordinate software delivery across IQVIA Connected Devices’ product teams, ensuring alignment of timelines, dependencies, risk management strategies, and release milestones. Act as a central point of contact for delivery status, blockers, and escalation across teams.
