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Clinical Trials jobs in Surrey Heath

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    • Previous experience managing clinical trials, studies or research projects.
    • Experience in a Medical Affairs, Study Coordinator or clinical research-related role…
    • Work collaboratively with research nurses, investigators, trial monitors and pharmacy colleagues to ensure the efficient delivery of clinical trials and…
    • View all Surrey and Borders Partnership NHS Foundation Trust jobs - Chertsey jobs - Pharmacy Technician jobs in Chertsey
    • Salary Search: Specialist Pharmacy Technician – Clinical Trials salaries in Chertsey
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    • Supports review and forecasting of inventory levels for all clinical trial supplies, in cooperation with project teams and project vendors.
    • Basic knowledge of Regulatory Guidelines and the clinical trial process .
    • Conduct and oversee study site monitoring visits to ensure compliance with protocols…
    • Strong understanding of country- and site-level budgeting strategies and clinical trial contracting principles.
    • Ensure timely communication of disclosure obligations to clinical teams, affiliates, and stakeholders.
    • Provide input on transparency obligations and best…
    • This role involves delivering temperature-controlled medication nationwide, primarily to patients in their homes, as part of our same-day delivery service.
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    • The Expanded Access Program Manager is responsible for the successful delivery of assigned programs from award through to close-out, ensuring all client…
    • To support training, competency, and accreditation, including intrathecal chemotherapy preparation, clinical trials setup, and mentoring colleagues within the…
    • The RRDN Director is the senior officer responsible for the overall leadership, delivery and management of the RRDN.
    • The establishment and delivery of the RRDN.
    • Experience within the pharmaceutical, healthcare, clinical trials, or transportation/logistics industry is an advantage.
    • Knowledge of the pharmaceutical, biotechnology, and/or clinical trial industry.
    • The Global Pricing Manager supports global operations by preparing pricing,…
    • Minimum 2 years of experience in clinical research, regulatory submissions, or site activation.
    • Collaborate with internal and external stakeholders, including…
    • ✅ Monitoring experience in clinical trials.
    • ✨ Exposure to advanced therapies – cell & gene, CAR‑T, innovative trial designs.
    • ✅ Monitoring experience in clinical trials.
    • ✨ Exposure to advanced therapies – cell & gene, CAR‑T, innovative trial designs.

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Job Post Details

Medical Affairs Coordinator - job post

Talentmark
4.9 out of 5 stars
BasingstokeHybrid work
£15.26 - £20.35 an hour - Fixed term contract

Job details

Pay

  • £15.26 - £20.35 an hour

Job type

  • Fixed term contract

Location

BasingstokeHybrid work

Full job description

Talentmark are recruiting for a Medical Affairs Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months from mid-September 2026.

Company:
Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.

Salary:
Paying from £15.26 - £20.35 per hour PAYE

Location:
This role allows hybrid working, based at our clients site in Basingstoke for 3 days per week, with 2 days working remotely.

Medical Affairs Coordinator Role:
  • Manage investigator-led research studies from start to finish, keeping everything on track and compliant
  • Be the go-to contact for colleagues, affiliates and external investigators, keeping communication clear throughout each study
  • Track timelines, enrolment and budgets, flagging any risks early
  • Help put together and manage research agreements and any changes to them
  • Keep study records and tracking systems accurate and audit-ready at all times
  • Handle the practical side of studies - supplies, paperwork, payments and purchase orders
Your Background:
  • Bachelor’s degree in a scientific or health-related field; OR at least 2 years’ clinical research experience.
  • Previous experience managing clinical trials, studies or research projects.
  • Experience in a Medical Affairs, Study Coordinator or clinical research-related role.
  • Experience with contracts, agreements, amendments or financial/administrative processes is desirable.
  • Strong written and verbal communication skills.
Apply:
For more information, or to apply for this Medical Affairs Coordinator role please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@talentmark.co.uk. Please quote reference 198988.

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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