The Contacts & Proposal Developer is responsible for reviewing Requests for Proposal (RFP) and preparing comprehensive proposal text and budgets. They also perform quality control edits and maintain corporate databases to ensure accurate tracking of opportunities.
The Senior Business Analyst will gather, analyze, and manage requirements for enterprise identity and access management solutions. They will collaborate with stakeholders to translate business needs into actionable requirements while ensuring alignment with security and regulatory standards.
The Proposal Developer will support the global sales organization by developing customer proposals, budgets, and pricing solutions for clinical research opportunities. They will collaborate with cross-functional teams to interpret customer requirements and ensure the accuracy and competitiveness of all proposal documentation.
The Junior Site Activation Coordinator supports and coordinates site activation activities for clinical research studies while ensuring compliance with regulations and project timelines. They are responsible for preparing regulatory documentation, tracking submissions, and maintaining internal systems to facilitate successful study start-up.
Direct and manage the delivery of site activation, maintenance, and regulatory activities for clinical studies. Oversee project timelines, budgets, and regulatory strategies while ensuring compliance with GCP and ICH guidelines.
The Clinical Trial Safety Scientist is responsible for the ongoing review of clinical and safety data to ensure medical accuracy and consistency. They also facilitate safety data meetings, contribute to study start-up activities, and collaborate with study physicians to support medical evaluation.
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 collaborate with study physicians to support high-level data evaluation and contribute to study start-up and safety reporting processes.
The Central Monitor performs centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations. They also manage site triggers, prepare site packs, and interact with cross-functional teams to resolve data issues.
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 Sales Support Analyst is responsible for maintaining CRM data integrity and supporting sales operations such as quoting, contracting, and billing. They will validate account information, perform quality checks, and assist sales teams with opportunity setup and order processing.
The role involves assisting with the preparation, documentation, and maintenance of clinical trial records, including the Trial Master File and Case Report Forms. You will collaborate with clinical teams to ensure accurate data flow, site compliance, and effective communication across research projects.
The Study 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 meet quality standards.
The Project Lead manages a portfolio of decentralized clinical trial projects, serving as the primary point of contact for sponsors, sites, and cross-functional teams. They are responsible for financial oversight, project delivery, quality management, and mentoring team members to ensure milestone achievement.
The Associate Consultant supports the design and delivery of patient-focused and outcomes research projects for healthcare and life sciences clients. They are responsible for conducting qualitative and quantitative research, synthesizing evidence, and managing cross-functional stakeholders to develop client-ready deliverables.
The Associate Medical Director acts as a global or regional medical advisor, providing support for protocol-related issues, patient safety, and eligibility determinations. They also perform medical reviews of adverse events, clinical study reports, and contribute to investigator meetings and team training.
The Business Process Analyst will analyze financial data, review contracts, and resolve chargeback claims to ensure accurate financial outcomes. They will also manage multiple accounts, validate data across systems, and collaborate with team members to meet project deadlines.
The Lead Generator is responsible for identifying and qualifying opportunities within a customer portfolio to support medical representatives. They will engage with healthcare professionals to schedule appointments and maintain accurate records of all interactions.
Conduct remote medical visits with neurologists and nephrologists to promote innovative therapeutic solutions. Build and maintain professional relationships while presenting scientific product information through digital tools.
Conduct remote medical visits to neurologists and nephrologists to promote innovative therapeutic solutions. Build and maintain professional relationships while presenting scientific product information using digital tools.
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 Finance Specialist will manage a portfolio of clinical research projects, ensuring accurate payment administration and adherence to financial SOPs. They are responsible for monitoring financial risks, reconciling project budgets, and providing high-level support to internal teams.
Conduct remote medical visits with neurologists and nephrologists to promote innovative therapeutic solutions. Build and maintain professional relationships while presenting scientific product information through digital platforms.
Conduct remote medical visits to neurologists and nephrologists to promote innovative therapeutic solutions. Build and maintain professional relationships while presenting scientific product information using digital tools.
The role involves assisting with the preparation, maintenance, and archiving of clinical trial documentation to ensure accurate Trial Master File delivery. You will also coordinate clinical data flow, support Clinical Research Associates, and act as a central contact for project communications.
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 Director will lead the creative vision and copy direction for healthcare and pharmaceutical brands, ensuring strategically grounded and scientifically accurate work. They will mentor creative teams, manage client relationships, and oversee the development of integrated campaigns from concept through production.
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 Lead Clinical Research Coordinator supports clinical research studies by performing remote clinical activities and managing patient data in compliance with protocols. They are responsible for recruiting and enrolling participants, ensuring study compliance, and maintaining accurate documentation throughout the trial lifecycle.
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.
The Survey Quality Assurance Specialist ensures the accuracy, functionality, and compliance of market research surveys through systematic testing and validation. They also monitor surveys during fielding, investigate data quality issues, and collaborate with cross-functional teams to resolve defects.
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.
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality execution.
The manager will design and deliver bespoke AI solutions for life sciences clients, leading multidisciplinary teams from use case discovery to production deployment. They will also provide technical leadership, mentor team members, and serve as the primary point of contact for client stakeholders.
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+.
The Site Activation Coordinator manages site identification, feasibility, and regulatory start-up activities for clinical trials. They serve as the primary point of contact for investigative sites, ensuring documentation is accurate and project timelines are met.
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 specialist will manage end-to-end site activities from feasibility to closure, serving as the primary point of contact for investigative sites. They are responsible for regulatory submissions, essential document tracking, and providing updates to cross-functional study teams.
The specialist proactively drives and executes start-up and maintenance activities for clinical studies and sites in Chile. They serve as the single point of contact for investigative sites and project teams while ensuring adherence to SOPs and project timelines.
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.
Lead clinical study delivery, coordinating cross-functional teams and ensuring studies meet contractual requirements, timelines, quality standards, and financial objectives. Manage customer and vendor relationships, risks, scope changes, project reporting, and team development while identifying opportunities to improve delivery.
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.
You will design, develop, and maintain scalable web applications with a primary focus on React-based front-end development. Additionally, you will collaborate with cross-functional teams to translate business requirements into effective technical solutions and provide production support.
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 are responsible for contacting insurance companies to verify eligibility, perform benefit investigations, and manage prior authorizations or appeals. They also directly assist patients and providers with enrollment in assistance programs and provide support via inbound and outbound calls.
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 specialist will manage coding and coverage inquiries while facilitating patient access through benefit investigations and claims appeals. They are responsible for maintaining accurate records in the CRM and providing proactive support to clients and healthcare providers.
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.
The VP, Management Director will serve as the senior strategic and operational lead for a major rare disease brand launch. They will nurture client relationships, drive organic growth, and mentor a cross-functional team to ensure high-quality service delivery.
The Virtual Key Account Manager will develop and grow customer accounts through effective virtual engagement with healthcare professionals and stakeholders. They will deliver compliant product education and create tailored business plans to drive the adoption of smoking cessation solutions.
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 Scientific Advisor develops high-quality scientific content and strategies to meet client objectives while partnering with internal teams and key opinion leaders. They facilitate advisory board meetings and provide scientific expertise to support product strategy and clinical study design.
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 Associate Director oversees end-to-end delivery, governance, and optimization of IQVIA information assets for key MedTech accounts. They serve as the primary point of accountability for client satisfaction, issue resolution, and driving incremental growth through expanded solution utilization.
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.
The analyst will review scientific literature to extract and maintain psychometric data within the COAA platform. They are also responsible for performing quality control checks to ensure the accuracy, consistency, and completeness of the data.
The Regulatory and Start-Up Specialist manages site identification, regulatory documentation, and contract negotiations to ensure clinical trial start-up activities are completed on time. They serve as the primary point of contact for investigative sites and ensure all activities adhere to SOPs and project requirements.
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 Regional Specialist acts as a liaison between clinical teams and investigator sites to support the execution of remote and decentralized trial visits. Responsibilities include managing visit logistics, ensuring documentation compliance, and providing operational support to research clinicians.
The analyst will manage clinical trial site payment portfolios, ensuring accurate and timely payments in accordance with financial SOPs. They will also perform project reconciliations, track financial metrics, and provide high-level customer service to internal project teams.
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 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 Site Manager is responsible for remote site monitoring activities to ensure study protocols, regulations, and sponsor requirements are met. They collaborate with cross-functional teams to manage site identification, start-up, and ongoing clinical data integrity.
The Principal Statistical Programmer develops and validates complex datasets and outputs while ensuring compliance with CDISC standards. They also provide technical guidance, mentor junior staff, and collaborate with cross-functional teams to optimize programming workflows.
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 Patient Recruitment Specialist coordinates the operational delivery of patient recruitment and retention services for clinical studies. They manage study documentation, track timelines, and collaborate with internal teams and external vendors to ensure compliance and project success.
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 Senior Director provides strategic regulatory leadership for drug development, managing global teams and guiding clients through US and European regulatory frameworks. They are responsible for developing regulatory business, supporting submissions, and ensuring high-quality, data-driven deliverables across the product lifecycle.
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 Key Account Representative is responsible for managing a territory, establishing relationships with healthcare providers, and achieving quarterly and annual sales goals. The role involves executing tactical sales activities, conducting in-person calls with decision-makers, and collaborating with internal teams to ensure client satisfaction.
The Oncology Overlay Sales Specialist will educate and promote oncology therapeutics to key stakeholders within an assigned territory. This role involves conveying complex clinical and access information while collaborating with cross-functional teams to meet patient needs.
The role involves developing coding scripts and automation tools to support the Evidence Synthesis practice and Centre of Excellence. You will also contribute to complex statistical projects and disseminate research outputs through peer-reviewed journals and conferences.
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 Central Monitor is responsible for the centralized review of study and site-level risk signals to ensure data quality and patient safety. They analyze clinical and operational data to identify trends and provide actionable recommendations to study teams and CRAs for risk mitigation.
The Medical Data Review Manager is responsible for reviewing structured clinical patient data to ensure medical plausibility and protocol adherence. They will identify data anomalies, verify adverse events, and ensure the overall readiness of patient information for subsequent review levels.
The specialist is responsible for independently drafting, reviewing, and negotiating clinical trial agreements to support study start-up activities. They act as a primary point of contact for investigative sites and internal stakeholders to ensure efficient contract execution and regulatory compliance.
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.
You will act as a liaison between clients and technical teams to define business use cases and translate analytical concepts into actionable recommendations. Additionally, you will manage multi-disciplinary projects, mentor junior staff, and support business development through client pitches and proposals.
The Centralized Monitoring Analyst is responsible for setting up and programming the Centralized Monitoring platform, including QTLs, KRIs, and data visualizations. They also support the Centralized Monitoring Lead in developing study-specific strategies and maintaining platform specifications.
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.
Conduct outbound calls to healthcare professionals to collect, verify, and record key information in the database. Perform match activities, documentation, and troubleshooting to ensure data accuracy according to project guidelines.
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 will conduct site feasibility assessments and investigator outreach across Poland, Hungary, and the Czech Republic. They will also support study start-up activities, including EU CTR document collection and essential site document review.
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.
The Data Acquisition Specialist is responsible for defining, setting up, and ingesting external data streams in alignment with clinical trial protocols. They will liaise with stakeholders and external providers to ensure data transfer agreements are accurate and compliant with regulatory standards.
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 operational excellence and business growth.
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.
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 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. 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 specialist will manage site activation activities and serve as the primary point of contact for investigative sites and project teams. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and tracking project timelines to meet clinical research objectives.
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 Director will drive global business development by identifying market opportunities and executing strategies for commercial outsourcing and engagement solutions. They will act as a strategic advisor to senior clients while leading complex, multi-country proposal development and cross-functional teams.
The Associate Director manages client relationships and leads account teams to ensure project deliverables meet operational excellence standards. They are responsible for driving organic business growth, mentoring staff, and maintaining alignment with company strategy and goals.
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.
The Medical Director provides medical, clinical, and scientific advisory expertise for clinical trials and business development activities. Responsibilities include medical monitoring, protocol review, safety oversight, and strategic support for client proposals.
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.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
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 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 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 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.
The Senior Business Analyst will lead the gathering, analysis, and validation of software requirements for the clinical eSource platform. They will collaborate with cross-functional teams to translate business needs into functional specifications and technical documentation.
The Database Operator will maintain and update product reference databases for the Norwegian market to ensure high data accuracy and integrity. They will also collaborate with local teams to resolve data discrepancies and contribute to continuous improvement initiatives.
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 Senior Business Analyst will lead the gathering, analysis, and validation of software requirements for clinical trial automation systems. They will collaborate with cross-functional teams to translate business needs into functional specifications and technical documentation.
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 Senior Medical Director provides scientific, clinical, and operational oversight for global clinical research programs while serving as the primary medical monitor. They are responsible for ensuring patient safety, interpreting clinical data, and guiding study teams through protocol execution and regulatory interactions.
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 Senior Safety Project Lead manages service delivery excellence for assigned projects, acting as the primary point of contact for internal and external customers. They are responsible for project planning, financial management, and ensuring compliance with regulatory requirements throughout the product lifecycle.
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 Client Services Director is responsible for managing client accounts, overseeing project timelines, and ensuring the scientific accuracy of deliverables. They also facilitate communication between internal departments and external stakeholders to drive long-term account planning and brand strategy.
The Global Clinical Project Manager is responsible for overseeing vendor activities across the study lifecycle to ensure high-quality deliverables and operational efficiency. They will manage vendor performance, track KPIs, and coordinate study start-up and close-out activities.
The Global Clinical Project Manager is responsible for overseeing vendor deliverables across the clinical trial lifecycle to ensure quality and efficiency. Key tasks include managing vendor performance, supporting site activation, and coordinating study close-out activities.
The specialist will manage the collection, review, and preparation of regulatory documentation for UK clinical trial submissions. They will also coordinate Informed Consent Form adaptations and liaise with investigative sites to ensure submission packages are compliant and timely.
The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
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.
You will design and develop software solutions using .NET and Java to support healthcare business processes. Additionally, you will be responsible for maintaining existing software, improving performance, and contributing to architectural decisions.
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 PV Safety Specialist is responsible for managing the collection, reporting, and oversight of safety information in compliance with global and local regulatory requirements. They also support the Local Pharmacovigilance Officer in maintaining safety risk management and ensuring inspection readiness across the affiliate.
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 Project Manager will serve as the primary point of contact for eCOA studies, managing project scope, timelines, and budgets. They will lead client meetings, oversee system changes, and ensure compliance with operational standards.
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.
Process and manage safety data and adverse events in accordance with regulatory guidelines and internal SOPs. Collaborate with functional team members and healthcare professionals to ensure quality and compliance across project deliverables.
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-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.
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.
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 input for clinical data and regulatory submissions.
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 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 card activation, verifying program eligibility, and troubleshooting submission rejections.
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 project teams to ensure site readiness.
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.
You will support the planning, execution, and monitoring of healthcare marketing campaigns while ensuring quality, traceability, and audit readiness. Additionally, you will focus on standardizing and automating repeatable tasks to improve operational efficiency and capacity.
The Central Independent Rater will administer, score, and review psychiatric assessments such as MINI and MADRS for clinical trials. They will work as part of a global team to support depression studies and ensure accurate clinical data collection.
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 Medical Information Case Processor is responsible for receiving and documenting incoming inquiries from patients and healthcare providers regarding safety data. They must also create accurate Adverse Event and Product Quality Complaint reports while adhering to regulatory guidelines and project requirements.
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 Associate Client Success Director serves as a strategic partner and primary point of contact for enterprise clients, ensuring they achieve measurable business outcomes through Cedar Gate solutions. This role involves leading cross-functional account teams, driving product utilization, and representing the voice of the client to inform product development.
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.
The Associate Business Development Director is responsible for prospecting, qualifying, and closing new business opportunities within medical specialty societies. This role involves developing comprehensive sales plans, managing the full sales cycle, and serving as a liaison between customers and internal technical teams.
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.
The Contract Negotiation Specialist is responsible for independently drafting, reviewing, and negotiating clinical trial agreements to support study start-up activities. They act as a primary point of contact for sites and internal teams while ensuring all contracts comply with regulatory requirements and project timelines.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with regulatory requirements. Manage study progress by tracking regulatory submissions, recruitment, and data query resolutions.
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 Centralized Monitoring Lead will oversee the Centralized Monitoring team and partner with project and clinical leads to ensure project objectives are met. Responsibilities include managing clinical deliverables, project resources, and developing monitoring strategies.
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.
Lead the vision, strategy, and roadmap for the Media OS platform to transform it into an AI-powered audience and activation ecosystem. Drive commercial growth and cross-functional leadership to deliver personalized, privacy-compliant healthcare marketing solutions.
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.
Manage the coordination, planning, and implementation of patient recruitment and retention operational plans for clinical studies. Act as the primary operational contact for sponsors and manage project budgets and KPIs to ensure study milestones are met.
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.
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.
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.
Lead the strategic and operational delivery of global site activation activities to accelerate patient enrollment. This includes managing site identification, regulatory submissions, and contracting in compliance with ICH-GCP standards.
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.
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
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.
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. 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. 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.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, recruitment, and data integrity across various therapeutic areas.
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 Principal Biostatistician provides statistical support for clinical trials, including authoring statistical analysis plans and producing efficacy analysis datasets. They also collaborate with multi-disciplinary teams and contribute to regulatory documents such as INDs and NDAs.
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.
The representative will serve as the primary contact for patients and healthcare professionals to assist with payment programs, card activation, and eligibility. They are responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
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.
Conduct nutritional assessments and develop personalized dietetic plans for clients via telecommunications. Provide ongoing dietetic counseling and support to clients and their families while maintaining accurate records.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
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.
