The Vendor Contracts Manager is responsible for the full life cycle of vendor contracts, including drafting, negotiating, and executing agreements. They also focus on process improvement and risk mitigation to ensure efficient and compliant business operations.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately and on time. Responsibilities include managing system access, maintaining project documentation, and assisting with the preparation and submission of trial-related files.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide guidance to site staff, manage site documentation, and verify source documents for patient safety and compliance.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to site staff and ensure all site-related documentation is accurately filed in the Trial Master File.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and management throughout the clinical trial lifecycle. They also provide mentorship to less experienced staff and ensure compliance with protocol, safety, and data integrity standards.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence. They also provide mentoring to less experienced staff and manage study documentation, including data verification and safety reporting.
The Global Organizational Learning & Development Coordinator manages the operational execution of training logistics, including scheduling, learner communications, and attendance tracking. This role serves as a central point of coordination for enterprise learning programs to ensure consistent delivery and a high-quality learner experience.
The Manager of Clinical Operations Site Management is responsible for overseeing assigned Clinical Research Associates to ensure performance, quality, and effective utilization. They handle recruitment, training, performance appraisals, and act as a point of escalation for project-related issues.
The Clinical Research Associate will conduct site visits including qualifications, initiations, and monitoring while ensuring compliance with safety and regulatory standards. They will also manage study documentation and actively participate in investigator meetings to support clinical trial success.
The Senior Clinical Trial Manager oversees clinical study site management activities, leading a team of clinical staff to ensure protocol compliance and data quality. They are responsible for monitoring study progress, managing site relationships, and coordinating global monitoring strategies throughout the study lifecycle.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements, informed consent, and safety reporting while managing site activities remotely.
The Senior Director will partner with the EVP of Global Quality to develop and execute global quality and compliance strategies across clinical research services. They will lead quality transformation initiatives, oversee regulatory inspections, and manage a team of quality leads to ensure operational excellence and inspection readiness.
The RTSM Specialist manages the implementation and lifecycle of Randomization and Trial Supply Management systems for clinical trials. They are responsible for project oversight, budget management, system design, and ensuring compliance with company standards and regulatory requirements.
The Senior Specialist is responsible for drafting, reviewing, and negotiating clinical research site contracts and budgets. They also facilitate the signature process and maintain tracking tools to ensure all project-related documentation is accurately managed.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCPs and regulatory standards. They also provide mentoring to less experienced staff, manage study deliverables, and ensure the quality and timely submission of clinical data.
The Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and oversee the collection of data and safety reporting throughout the study lifecycle.
The Senior Salesforce Architect serves as the enterprise design authority, owning the technical roadmap and development standards for the Salesforce and Certinia ecosystem. This role leads the integration of AI-driven capabilities and manages a team of administrators and developers to support commercial business outcomes.
The Director leads the evolution of the finance technology stack and data architecture to integrate AI and intelligent automation across global finance functions. They are responsible for managing the multi-year transformation roadmap, overseeing cross-functional projects, and ensuring alignment with business objectives.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring compliance with regulatory requirements and managing safety-related event reporting.
The RTSM Specialist manages the implementation and decommissioning of RTSM systems, ensuring deliverables meet client requirements and company standards. They serve as the primary escalation point for project issues and oversee study design, budget, and vendor work orders.
The associate manages the full spectrum of vendor and client invoice processing, including accounts receivable and accounts payable functions. Responsibilities include reconciling accounts, preparing financial reports, ensuring compliance with internal policies, and assisting with audits and tax filings.
The Senior Site Activation Manager oversees site activation project management, including site identification, regulatory document collection, and contract status monitoring. They serve as the primary point of accountability for study start-up activities, ensuring all tasks are completed on time and within budget.
The Clinical Trial Manager is responsible for leading clinical study site management activities and ensuring compliance with study protocols and SOPs across a geographic region. They will oversee site monitoring, manage project deliverables, and provide leadership to clinical staff to ensure high-quality data and timely study execution.
The Clinical Trial Liaison manages strategic relationships with clinical investigators and site staff to ensure successful trial execution and high-quality endpoints. They provide scientific and operational guidance to project teams while proactively managing site performance and protocol compliance.
The Clinical Research Associate is responsible for overseeing clinical trial activities to ensure quality and adherence to protocols. They work collaboratively with global teams to support the mission of improving patient lives through innovative research.
The Associate eCOA Manager provides project management oversight for eCOA studies, ensuring deliverables meet SOP standards and timelines. They serve as the primary escalation point for study-related issues and manage financial reviews, budget tracking, and vendor coordination.
The specialist serves as the primary point of contact for regulatory submissions, site activation, and maintenance activities for assigned clinical projects. They are responsible for planning, tracking essential documents, and ensuring compliance with ICH GCP and local regulatory requirements.
The Associate eCOA Manager provides project management oversight for eCOA studies, ensuring deliverables meet SOP standards and timelines. They serve as the primary escalation point for study-related issues and manage financial reviews, budget tracking, and vendor coordination.
The Investigator Grants Specialist is responsible for the development, delivery, and maintenance of investigator grants during both the bidding and template development phases of clinical studies. They also provide strategic advice on forecasting and risk mitigation to internal departments and stakeholders.
The analyst will support the modernization of pricing solutions by gathering business requirements, documenting workflows, and performing data analysis. They will also execute testing, quality assurance, and user acceptance validation to ensure the integrity of pricing and budgeting tools.
The Organizational Learning Advisor designs, delivers, and maintains global systems training for critical clinical and enterprise technology platforms like Medidata and Certinia. They partner with cross-functional stakeholders to translate complex workflows and compliance requirements into effective role-based learning experiences.
The Organizational Learning Advisor will build and lead the commercial learning and enablement strategy from the ground up to support revenue growth and client satisfaction. This role involves designing curricula, facilitating training, and partnering with commercial leaders to identify capability gaps and drive behavioral transformation.
The Proposal Manager leads the development of high-quality FSP proposals across various functional service lines including Biometrics and Clinical Operations. They are responsible for coordinating internal strategy meetings, managing proposal timelines, and collaborating with Business Development and Finance to ensure accurate pricing and deliverables.
The Senior Clinical Trial Liaison manages strategic relationships with clinical investigators and site staff to ensure successful trial execution and quality endpoints. They provide operational guidance to project teams, monitor site performance, and proactively manage issues related to protocol adherence and patient enrollment.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
The Associate is responsible for preparing and rendering client invoices, managing pass-through cost reimbursements, and reconciling billing reports. They also assist with expense claim reviews, process gap identification, and support annual corporate audits and tax filings.
The Clinical Scientist is responsible for the review, interpretation, and assessment of clinical data to ensure high-quality reporting and study integrity. They collaborate with cross-functional teams to manage protocol-defined variables, track safety events, and present key findings to clients and medical monitors.
The Executive Director of Project Management oversees the direction of the project management team, including financial performance, resource management, and strategic business acquisition. They are responsible for maintaining effective client relationships, leading sub-therapeutic groups, and ensuring project deliverables meet sponsor expectations.
The Senior Director of Business Development is responsible for achieving revenue objectives by identifying new business opportunities and building productive client relationships within the clinical research industry. They will lead proposal development, conduct bid defense presentations, and coordinate strategic account growth while managing interactions between sponsors and internal project teams.
The manager oversees and coordinates all business development activities within the Biometrics and Pharmacovigilance department, including bids, proposals, and change orders. They are responsible for triaging proposals, developing budgets, and ensuring consistency in departmental documentation and strategy.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and regulatory compliance. They are responsible for overseeing site performance throughout the study lifecycle and ensuring adherence to safety and protocol requirements.
The Director of Proposals serves as a subject matter expert for Functional Service Provider (FSP) solutions, leading the full-cycle development of complex proposals and budgets. They collaborate with cross-functional teams to define strategy, manage client deliverables, and ensure the successful submission of proposals.
The Senior Clinical Research Associate manages research activities at sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
The Clinical Payments Associate manages administrative tasks, including triaging tickets and emails, and supports financial workflows within the clinical research team. They also assist with system migrations and study reconciliation activities by maintaining trackers and organizing documentation.
The Senior Clinical Payments Specialist manages end-to-end global investigator grant payments, including setup, deployment, and close-out of payment solutions. They are responsible for reconciling payments, analyzing budget versus actual spend, and acting as a primary point of contact for payment-related queries.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between clinical research teams and sites while ensuring payments align with contract terms and budgets.
The role involves processing, reviewing, and resolving Trial Master File (TMF) documents while ensuring adherence to regulatory standards and industry best practices. You will perform periodic quality control checks and collaborate with project teams to maintain essential clinical research documentation.
The Associate Director will oversee the clinical data management team to ensure compliance with SOPs, project budgets, and quality standards. They are responsible for providing strategic leadership, managing departmental deliverables, and implementing process improvement initiatives.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation of study payment solutions. They act as a liaison between investigative sites and clinical teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Senior Recruiter is responsible for developing and executing end-to-end recruitment strategies, including sourcing, screening, and selecting high-caliber candidates. They also manage hiring manager relationships, oversee the offer process, and ensure compliance with legal requirements.
Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The Senior Statistician manages statistical project support and provides expert consultancy across clinical trial programs. Responsibilities include developing SAS programs, writing statistical analysis plans, and ensuring compliance with regulatory standards.
The Site Activation Specialist tracks regulatory documents and manages communication with clinical research sites to ensure timely study start-up. They also support site identification activities, including the negotiation of agreements and the review of site feasibility questionnaires.
The Clinical Payments Specialist manages end-to-end investigator payments, ensuring alignment with clinical trial agreements and budgets. They act as a primary point of contact for payment-related queries and perform regular reconciliations and financial reporting.
The Clinical Payments Associate manages administrative tasks, processes payment queries, and maintains accurate financial records within clinical trial systems. They also support system migrations and study reconciliation activities by organizing documentation and tracking project progress.
The Principal Biostatistician assists in designing clinical studies, preparing statistical analysis plans, and interpreting data from pharmacokinetic and clinical trials. They also provide scientific leadership, supervise personnel, and collaborate with interdisciplinary teams to ensure high-quality documentation.
The Senior Director of Project Management is responsible for the overall direction and financial performance of the project management team within a therapeutic group. They oversee project plans, manage client relationships, and lead the recruitment and development of personnel.
The RTSM Specialist provides project management oversight for RTSM study lifecycles, ensuring deliverables meet quality standards and timelines. They serve as the primary escalation point for project issues and manage study budgets, vendor work orders, and system design specifications.
The Associate Director of Project Management oversees large, multi-national clinical projects and provides functional leadership, training, and mentoring to Project Managers. They are responsible for ensuring project deliverables meet cost, time, and quality requirements while serving as a key liaison for clients and internal stakeholders.
The specialist serves as the primary point of contact for site identification, activation, and maintenance activities for clinical projects. They are responsible for managing regulatory submissions, ensuring compliance with ICH GCP guidelines, and tracking essential study documents.
The Senior Workday Administrator will own the configuration, maintenance, and security of Workday HCM and Advanced Compensation modules. They will also lead system upgrades, perform advanced troubleshooting, and act as a liaison between departments to ensure process efficiency and data integrity.
Implement, configure, and maintain pricing tools and automated systems to support commercial solutions and modernization initiatives. Collaborate with cross-functional teams to define technical requirements, perform code reviews, and ensure data integrity across pricing platforms.
The Salesforce Administrator will lead the ongoing development, configuration, and maintenance of the Salesforce platform to optimize business processes. They will collaborate with cross-functional teams to design, test, and deploy enhancements while ensuring data integrity and providing user support.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to site staff and manage study documentation within the Trial Master File.
Provide leadership and direction to the clinical site management team from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The role involves managing safety management plans, reviewing SAE data for accuracy, and performing data entry into safety databases. Additionally, the associate will generate regulatory reports and ensure compliance with safety regulations throughout the clinical drug development lifecycle.
The In-house Clinical Research Associate II manages site-related tasks, including documentation, regulatory compliance, and EDC query resolution in accordance with GCP and SOPs. They also provide support to field CRAs and project teams to ensure study deliverables are met within contracted timelines.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The In-house Clinical Research Associate II manages site-related tasks, ensures compliance with GCP and SOPs, and supports clinical trial managers and field CRAs. They are responsible for TMF maintenance, remote monitoring, site communication, and assisting with study documentation and data queries.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety-related event reporting.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The Medical Writer II is responsible for preparing and leading the medical writing team on Phase I-IV study documents, including protocols, clinical trial reports, and investigator brochures. They must ensure all documentation meets regulatory, scientific, and ethical standards while coordinating review cycles with sponsors.
The Category Vendor Manager oversees clinical vendor performance to ensure supply security, safety, and compliance with SLAs and quality standards. They manage vendor relationships, monitor performance metrics, and lead continuous improvement initiatives across the organization.
Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
Provide leadership and direction to the clinical site management team from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The Site Activation Manager is responsible for overseeing site activation and start-up activities for oncology clinical trials to ensure milestones are met on time and within budget. They coordinate cross-functional teams, manage site identification and regulatory documentation, and provide input for business development proposals.
The Associate Manager is responsible for interviewing, selecting, and onboarding CRA/IHCRA candidates while ensuring they are properly trained and mentored. They also manage performance, review quality metrics, and act as a point of escalation for project-related issues.
The Project Manager is responsible for the overall coordination and management of clinical trials from startup through closeout. They lead core project teams and manage technical, financial, and operational aspects to ensure deliverables meet time, quality, and cost expectations.
The Grants Payable Specialist is responsible for processing site and investigator payments while managing accounting functions like reconciliations and month-end closing. They also handle tax reporting, vendor master data maintenance, and address payment-related queries.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory authorities and provide strategic guidance to project teams.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety-related event reporting throughout the study lifecycle.
The Senior Associate will manage complex TMF activities, oversee quality control processes, and ensure compliance with regulatory standards. They will also act as a subject matter expert, collaborating with project teams and sponsors to maintain essential clinical trial records.
Develop, test, and execute SAS programs to produce CDISC SDTM and ADaM datasets, tables, figures, and listings. Serve as a programming project lead for medium complexity studies while ensuring data quality and regulatory standards are met.
The RTSM Specialist provides project management oversight for RTSM study lifecycles, ensuring deliverables meet SOP standards and timelines. They act as the primary point of contact for stakeholders and manage study design, budget, and system validation activities.
The Clinical Trial Manager is responsible for leading clinical study site management activities and coordinating a team of clinical staff within a geographic region. They ensure site qualification, initiation, monitoring, and close-out activities are conducted in compliance with study protocols and standard operating procedures.
The Site Activation Manager is responsible for coordinating and overseeing site identification, essential document collection, and contract status for clinical trials. They ensure all start-up activities are completed on time and within budget while maintaining compliance with GCP and local regulations.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing rescue strategies when necessary.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are performed accurately. Responsibilities include managing system access, maintaining project documentation, and performing quality audits on trial files.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing contingency plans as needed.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
The specialist will manage, compile, and submit regulatory documentation while ensuring compliance with ICH GCP and local requirements. They will also act as a liaison for translation reviews and maintain country-specific patient information and labeling.
The Principal Statistician will design clinical trials, write Statistical Analysis Plans, and provide statistical leadership across various therapeutic areas. They will also develop and validate SAS programs for statistical analysis while ensuring compliance with regulatory standards and sponsor requirements.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements, manage informed consent processes, and oversee safety-related event reporting.
The Manager, Regulatory Affairs provides expert regulatory guidance throughout the drug development cycle and oversees the compilation and submission of regulatory dossiers. They are also responsible for mentoring junior staff, managing departmental work practices, and ensuring compliance with international regulations.
The Director serves as the single point of contact for a portfolio of EPMO projects, driving strategic planning, problem-solving, and value realization. They also coach project leaders, facilitate executive governance, and champion the integration of AI into project methodologies.
The specialist will analyze PSC workflows to identify inefficiencies and implement automation solutions to improve operational performance. They will also translate complex data into actionable insights and KPIs to support leadership decision-making.
The Contract Manager is responsible for the full life cycle of sponsor contracts and change orders, including drafting, budget preparation, and negotiation. They collaborate with internal departments such as Legal, Finance, and Operations to ensure compliance and accurate project scope definition.
The role involves processing, reviewing, and maintaining Trial Master File (TMF) documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Senior Clinical Trial Manager oversees clinical study site management activities and leads a team of clinical staff on complex global studies. They are responsible for ensuring site qualification, initiation, monitoring, and close-out activities while maintaining data quality and project timelines.
The Grants Payments Data Analyst will build and maintain forecasting models for clinical site payments while collaborating with cross-functional teams to ensure financial accuracy. They are responsible for creating client-ready deliverables, performing variance analysis, and ensuring compliance with audit requirements.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide mentoring to less experienced staff and maintain accurate documentation for the Trial Master File.
The Vice President of Corporate Development will lead the company's global inorganic growth strategy, including mergers, acquisitions, and strategic partnerships. They will manage end-to-end deal execution and coordinate cross-functional teams to ensure successful post-merger integration and value creation.
The role involves processing, reviewing, and maintaining essential clinical trial documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Director will oversee the delivery of clinical projects within cost, time, and quality requirements while providing direct supervision and mentoring to project managers. They will also collaborate with the Business Development team on proposals and contribute to the continuous improvement of business processes.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility assessments and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility management and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory intelligence and provide strategic advice to project teams regarding submission processes.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and data integrity while overseeing site performance throughout the study lifecycle.
The Sales Development Account Manager is responsible for sourcing new sales opportunities through inbound lead qualification and outbound prospecting. They will collaborate with Business Development partners to manage territories, set appointments, and drive leads through the early stages of the sales process.
The Senior Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet customer expectations.
The Vendor Contracts Manager is responsible for the full life cycle of vendor contracts, including drafting, reviewing, and negotiating agreements. They also focus on process improvement and risk mitigation to ensure efficient contract administration and compliance with company policies.
The Senior Legal Contract Manager is responsible for independently reviewing, redlining, and negotiating sponsor-facing legal and commercial contracts. They will manage the full contract lifecycle while collaborating with internal stakeholders to ensure alignment on business, legal, and operational requirements.
The Associate will process, review, and resolve Trial Master File (TMF) documents while ensuring compliance with SOPs and industry regulations. They will also provide administrative support to the RMC Lead, including maintaining quality control checklists and tracking study documentation.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.
The analyst will prepare financial metrics and reports for internal management while enhancing business tools to automate processes. Key duties include project setup, ERP data integrity maintenance, and managing the timekeeping and billing processes.
The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.
Oversee and lead data management services across multiple complex global clinical projects from start-up to closeout. This includes preparing trial documentation, managing database locks, and coordinating with internal departments and sponsors.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Independently manages statistical project support and provides expert consultancy for clinical trial designs and analysis plans. Develops and runs SAS programs for data reporting while ensuring compliance with regulatory standards like FDA and ICH.
Lead the writing, coordination, and presentation of robust proposals for assigned projects. Collaborate with Account Directors and subject matter experts to manage the proposal development process and ensure accurate service offerings.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event (SAE) data according to regulatory guidelines. The role involves authoring Safety Management Plans and performing quality control on safety data processed by other associates.
Independently manage statistical project support and provide expert consultancy for clinical trial designs and analysis plans. Develop and run SAS programs for data reporting while ensuring compliance with regulatory standards like FDA and ICH.
The Medical Director provides medical management and professional support for clinical research projects as a Medical Monitor. Responsibilities include managing clinical trials, processing Serious Adverse Events, and contributing medical input to study protocols and development programs.
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The CRA is responsible for managing the full lifecycle of clinical sites, including qualification, initiation, monitoring, and close-out visits. They ensure protocol adherence, verify source documents for data veracity, and manage site documentation within the Trial Master File.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.
Responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. The role involves ensuring protocol adherence, verifying source documents, and mentoring less experienced CRAs.
Manage complex studies or sponsor portfolios by performing RMC Lead activities and providing subject matter expertise on TMF needs. Oversee quality control processes, develop TMF quality management documents, and present KPI trends to project teams and sponsors.
The Oncology Therapeutic Strategy Lead serves as a therapeutic consultant, supporting the Business Development organization and Therapeutic Area Leads. This role involves creating effective delivery strategies for clinical trials and collaborating with various internal teams to achieve new business targets.
Accountable for site activation project management and delivery within the Oncology therapeutic area, including oversight of site identification and regulatory activities. Responsible for tracking metrics, managing budgets, and communicating status and risks to sponsors and internal leadership.
The Senior Project Manager coordinates clinical trials from start-up through closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure all project deliverables meet customer time, quality, and cost expectations.
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Drive revenue growth by proactively marketing CRO services and identifying new leads for clinical, bioanalytical, and ADME business. Manage the full sales cycle, including writing proposals, delivering client presentations, and maintaining CRM data.
Accountable for directing multiple clinical projects simultaneously to ensure delivery within cost, time, and quality requirements. Acts as a liaison for business development and collaborates across functional areas to improve business processes.
The Senior Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Oversee operational activities for Clinical Assessment Technologies (CAT) projects, including resource management and vendor oversight. Lead departmental initiatives, manage study deliverables from launch to close-out, and support business development activities.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up activities, and regulatory document collection. Conduct study initiation visits and ensure compliance with informed consent and safety reporting throughout the study lifecycle.
The specialist will plan, implement, and monitor the overall study supply chain strategy to maximize efficiency and minimize costs. This includes managing inventories of study drugs and collaborating with project management and vendors to optimize delivery processes.
The Specialist manages the end-to-end proposal process, including the preparation of RFPs, RFIs, and complex budget tools. They collaborate with account directors and operational teams to refine scopes and ensure comprehensive client service delivery.
The role focuses on sourcing new sales opportunities through inbound lead qualification and outbound prospecting to drive revenue growth. The manager will engage prospects, set appointments for Business Development partners, and manage sales territories using Salesforce.
The Associate Director of FP&A supports complex financial planning, reporting, and analysis to drive data-driven decision making. Key duties include producing monthly board reports, managing forecasts and budgets, and partnering with corporate functions to achieve financial targets.
Manage and track regulatory submissions for clinical trials in Poland, ensuring compliance with EU-CTR and local regulations. Liaise with project teams to provide strategic guidance on documentation, labeling, and patient consent forms.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including identification, start-up, maintenance, and close-out phases. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Lead the operational strategy and growth objectives for global regulatory affairs, overseeing the delivery of regulatory activities and supporting roles. Drive business development efforts by contributing to proposals, bid defense meetings, and regulatory costing for site activation strategies.
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Lead the architecture, engineering, and operational delivery of enterprise Identity and Access Management (IAM) capabilities. Design and implement scalable identity solutions and automate lifecycle processes across a global, regulated environment.
The Architect serves as the enterprise owner and strategic leader for the Workday Adaptive Planning platform, overseeing the product vision and roadmap. They partner with Finance and HR leadership to design secure, high-performing models and integrations aligned with business strategy.
Responsible for managing all stages of clinical research activities at study sites, including qualification, initiation, monitoring, and close-out. Ensures data quality and compliance with GCP, local regulations, and SOPs while managing safety event reporting.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team. Key duties include maintaining project portals, managing trial master files, and coordinating project-specific training.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
The Senior Project Manager coordinates clinical trials from start-up to closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure project deliverables meet customer expectations regarding time, quality, and cost.
Liaise with colleagues to organize and submit high-quality regulatory submissions on a timely basis. Maintain country-specific patient information, consent forms, and drug labeling to ensure compliance with ICH GCP and local requirements.
The Senior Clinical Research Associate is responsible for site qualification, monitoring, and management to ensure protocol adherence and data integrity. They also provide mentorship to less experienced staff and ensure all site documentation is accurately filed in the Trial Master File.
The Clinical Scientist leads the assessment of clinical data to ensure quality and integrity while translating complex findings into actionable insights for internal teams and clients. They collaborate with cross-functional stakeholders to support regulatory deliverables, monitor safety events, and drive study execution strategies.
The Risk and Central Monitoring Manager coordinates cross-functional risk management and central monitoring activities for clinical trials in accordance with ICH GCP guidelines. They are responsible for developing monitoring strategies, overseeing risk-based quality management activities, and ensuring inspection readiness throughout the study lifecycle.
The Senior Director of Business Development is responsible for driving revenue growth by identifying new business opportunities and managing client relationships within the clinical research industry. They lead proposal development, conduct bid defense meetings, and coordinate strategic interactions between sponsors and internal project teams.
The Director of Business Development is responsible for achieving revenue objectives by identifying new business leads and managing client relationships within the clinical research industry. They will lead proposal development, conduct bid defense meetings, and coordinate strategic efforts with internal teams to secure new contracts.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet time, quality, and cost expectations.
The Senior Associate will perform RMC lead activities for studies, including TMF set-up, maintenance, and coordination between project teams and eTMF administrators. They will also oversee quality control processes, monitor TMF metrics and KPIs, and provide support during regulatory and sponsor audits.
The Senior Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up to closeout. They oversee the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
The Clinical Scientist leads the review and assessment of clinical oncology data to ensure quality, integrity, and regulatory compliance. They collaborate with cross-functional teams to interpret clinical findings, monitor safety events, and support the development of key regulatory deliverables.
Manage research activities at clinical sites, including study start-up, site training, and maintenance. Ensure compliance with regulatory requirements and oversee the collection of data and safety reporting throughout the study lifecycle.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
The Vice President of Business Development leads a team of account directors to drive sales targets and execute sponsor engagement strategies. This role is responsible for mentoring staff, managing performance, and collaborating with internal stakeholders to support the company's growth in the CRO market.
The Director will engage with senior management to establish strategic department initiatives and drive business development activities for Clinical Assessment Technologies. They are also responsible for overseeing the development of assessment training content and ensuring all materials meet protocol and regulatory requirements.
The Associate II is responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event data in accordance with regulatory guidelines and SOPs. They also serve as the Lead PV Associate for studies, authoring safety management plans and performing quality control on safety information.
The specialist will track study-specific site regulatory documents, follow up on necessary actions, and support the development and review of country/site-specific informed consent forms. Responsibilities also include maintaining communication with sites for timely start-up activities and collecting/reviewing essential regulatory documents.
The Sales Development Account Manager engages with prospective clients and internal stakeholders to build an effective new business pipeline, partnering with Business Development to achieve territory targets and goals. Key tasks include sourcing new sales opportunities through lead qualification and outbound prospecting, maintaining the prospect database, and achieving lead generation goals.
The Director of Business Development will achieve individual revenue and sales objectives by proactively communicating and selling Worldwide Clinical Trials' late-phase services to assigned clients. This role involves connecting the Worldwide team to established networks, identifying new leads for Phase II-IV business, and developing growth and retention strategies for the client base.
The role involves leading the migration of SQL Server and PostgreSQL workloads to Azure SQL Database and Azure SQL Managed Instances, alongside designing, deploying, and supporting PaaS and DBaaS offerings in Azure. Responsibilities also include analyzing and consolidating database instances for optimization and implementing native Azure backup, replication, disaster recovery, and security configurations.
