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Study Physician - Remote - UK

Posted 14 weeks ago
All others
Full Time
United Kingdom

Overview

Parexel is seeking an experienced Study Physician to contribute to clinical trials, providing medical oversight and ensuring high-quality protocols.

In Short

  • Work as a Study Physician dedicated to one client.
  • Provide medical expertise throughout the clinical trial phases.
  • Ensure timely preparation of clinical trial protocols.
  • Integrate medically relevant data into quality and risk management plans.
  • Co-author Clinical Quality Monitoring plans.
  • Perform ongoing reviews of medical data.
  • Minimum 4 years of clinical practice experience required.
  • Specialization in internal medicine or general practice is desirable.
  • Experience in the pharma industry or CRO is a plus.
  • Understanding of ICH-GCP regulations is essential.

Requirements

  • Physician (MD) with clinical training.
  • Experience in clinical development or pharmacovigilance is preferred.
  • Familiarity with data visualization systems and IT systems.
  • Strong understanding of relevant regulations and guidance.

Benefits

  • Opportunity to work with a leading CRO.
  • Contribute to improving global health.
  • Work in a collaborative and empathetic environment.
  • Engage in meaningful clinical development projects.

P.I.L

Parexel International Limited

Parexel International Limited is a leading global clinical research organization (CRO) dedicated to improving the world's health through innovative drug development solutions. With a strong commitment to patient well-being, Parexel supports clinical studies across a wide range of therapeutic areas, including oncology, and has played a pivotal role in the trials of many of today's top-selling drugs. Headquartered near Boston, Massachusetts, and in Durham, North Carolina, the company employs over 16,000 professionals and operates in more than 100 countries, providing comprehensive drug development capabilities, regulatory expertise, and advanced commercialization services to ensure efficient and effective clinical trial execution.

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