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The Candidate Development (Sourcing) Specialist is responsible for candidate management and building a pipeline for various aligned requisitions through active sourcing channels, including job boards,
Key Requirements: MBBS or MD from a recognized medical school 2+ years of experience in ICSR medical review Good understanding of medical terminology Experience in pharmacovigilance, drug safety, or c
Key Accountabilities : Programming / Software Development: Design, code, test, correct and document complex programs and scripts from agreed specifications, and subsequent iterations, using agreed sta
Key Responsibilities : MuleSoft Development (Primary Focus): Design and implement API-led connectivity solutions using MuleSoft Anypoint Platform to integrate internal and external clinical systems. D
Site Start Up EUCTR II Responsible for planning and submitting the complex EUCTR submission i.e. large phase II and III trials with multiple countries and sites. Job Requirements: In addition to the c
The MLR Technical Reviewer will be responsible for completion of tasks in the MLR Platform of Veeva Vault PromoMats and Veeva Vault Medical, the tasks will be related to the role of Content Administra
Responsibilities Conduct literature search on PubMed, and/or other subscribed databases; and validate relevant inclusions Create or update an existent gSSRCs/FAQs based on provided template or as per
Program Coordinator – Medical Communications Provide highly skilled, proactive project coordination support to assigned account teams and allocated projects to ensure efficient and effective project m
Key Accountabilities : Quality Management System (QMS)Support processes Support the execution of Parexel Quality's strategy and Parexel's QMS As assigned, support execution of the strategic and tactic
Key Accountabilities : Lead, Perform and Report audits Independently lead, plan, schedule, perform, and report a range of GxP audits across all phases of Clinical Research which may include but are no
Key Accountabilities : Proposal Development: Receives and analyzes Requests for Proposals (RFPs) documentation including study protocol or synopsis and ensures all appropriate Subject Matter Experts (
Key Accountabilities : Build Grant Estimate Timely preparation of accurate and competitive Clinical Study grants (Phases I – IV for all clinical indications) via proficient usage of any Clinical Study
Key Accountabilities : Site Contracts Associate Tasks Draft, review and negotiate all site agreements including but not limited to clinical study agreements, service agreements, team member agreements
Lead end-to-end signal management activities including detection, validation, evaluation, tracking, and closure Perform and oversee qualitative and quantitative signal analysis across clinical, post-m
The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational data to support the Data Surveillance process and reviewing project-specific Quality Tolerance Limits. They
Parexel is looking for a Senior Proposals and Contracts Specialist who has a solid knowledge of proposals and contract management principles and strong previous experience in project support, contract
The application analyst responsibility is to work with the Oracle EBS Finance 12.2.14 systems functions and other systems of the company related to finance and to ensure it aligns with the business ob
Contribute to the development of health economic models that evaluate the cost-effectiveness of health technologies for global reimbursement applications. Perform data analysis, assist in model buildi
Key Responsibilities: Workday HCM Maintain and enhance Workday Core HCM, including worker data, organizations, positions, compensation, and job architecture. Support end‑to‑end lifecycle processes: hi
The Director, Client Technology Partner (CTP) provides strategic leadership across key client accounts, ensuring technology solutions align with client objectives, operational needs, and business outc
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