Regulatory Affairs Specialist
Ensure compliance with regulatory requirements for drug approvals and submissions. Category: Regulatory Mode: Hybrid Responsibilities: Prepare regulatory submissions Liaise with authorities Track regu
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Quality Assurance Associate
Maintain quality standards in pharmaceutical manufacturing and processes. Category: Quality Control Mode: On-site Responsibilities: Conduct audits Ensure GMP compliance Document quality processes Requ
Biostatistician
Analyze clinical data using statistical methods to support research and development. Category: Data Science Mode: Remote Responsibilities: Design statistical models Analyze trial data Generate reports
Biostatistician manager
Analyze clinical data using statistical methods to support research and development. Category: Data Science Mode: Remote Responsibilities: Design statistical models Analyze trial data Generate reports
Candidate Development Specialist / Sourcing Specialist
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,
Senior Physician, Patient Safety
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
Senior Power Apps Developer
Key Accountabilities : Programming / Software Development: Design, code, test, correct and document complex programs and scripts from agreed specifications, and subsequent iterations, using agreed sta
Integration Engineer
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
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
Scientific Specialist-Medical Information
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
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
Quality Management System Oversight Lead
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
Senior Technology Auditor, QA
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
Study Grant Analyst II
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
Senior Manager, Medical Writing Services
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
Data Surveillance Analyst
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
Health Economics Associate- Modelling
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
Workday Payroll & HCM Developer
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
Director, Client Technology Partner
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
Health Economics Consultant
The Evidence Evaluation team is part of the Health Economics and Outcomes Research team (HEOR) within the Access Consulting business unit. The primary purpose of this job is to support the delivery of
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