Senior Clinical Study Specialist

4796828
  • Job type

    Contract
  • Location

    London
  • Working Pattern

    Full-time
  • Specialism

    Clinical Research
  • Industry

    Scientific and R&D
  • Pay

    Day rate

Senior Study Specialist 6 month hybrid role

Senior Study Specialist – 6 months in scope hybrid role (London)
The Senior Study Specialist supports the delivery of clinical trials by overseeing study activities, vendor performance, and site operations. Working closely with the Study Manager or Programme Lead, the role helps ensure studies are completed on time, within budget, and in compliance with regulatory and quality standards.
Key responsibilities include supporting study documentation, contributing to site feasibility and selection, overseeing CRO activities such as IRB/EC submissions, and managing essential documents across the study life cycle. The role also involves supporting investigator training,
maintaining
Trial Master File (TMF) quality, ensuring
accurate
ClinicalTrials.gov updates, and coordinating meetings with internal teams and external partners.
The Senior Study Specialist plays a key role in vendor oversight, including
Monitoring performance, managing budgets and invoices, and resolving escalations. They also contribute to risk identification and mitigation and support strong relationships with investigators and cross-functional teams.
Candidates should have experience in clinical operations within a pharmaceutical or biotechnology environment, with exposure to vendor management, study execution, and compliance processes.
Please send CV to Claire.helliwell@hays.com

Apply for this job

Talk to Claire Helliwell, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone 0333 010 6303
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