Quality , Science, Pharmaceutical & Food
Study Manager
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Contract
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London City, London, UK
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42076312
Desired Skills: Clinical trial management,Site management,Vendor oversight,Regulatory documentation,Veeva,RAVE,eCOA,IRT,CTMS,Cross-functional collaboration,Issue escalation,Study start-up,Monitoring oversight,Risk management,GCP compliance,Communication sk
PE Global is recruiting a Study Manager for our biopharmaceutical client based in London. The rate for this role is £340 per day Umbrella.
Location: Hybrid – 2 days/week in Holborn office (Wednesday + one additional day).
Contract Length: Initial 23 month contract.
Start Date: Ideally early November.
About the Role
We are seeking a Senior Study Specialist to join our clients Global Study Operations (GSO) team, supporting the execution and oversight of clinical trials. This is a hybrid contract position created as a backfill for a contractor converting to a full-time employee. The role has strong potential for extension and future full-time conversion, depending on business needs. You will play a key role in site and vendor management, contributing to activities that directly impact participant safety, data integrity, timelines, and study quality. This position requires a high level of independence, leadership, and communication, as well as the ability to handle complex vendors, sites, and regional oversight.
Key Responsibilities
- Oversight of site monitoring and management activities
- Management of study vendors and related issue escalations
- Support and execution of study documentation and operational plans
- Lead or contribute to activities delegated by Study Manager or Program Lead
- Maintain strong relationships with CROs and Key Principal Investigators
- Provide support or coverage for Study Manager as needed
What We’re Looking For
- 3–5 years’ experience in clinical research, ideally with regional lead experience in a sponsor or CRO setting
- Proven ability to work autonomously and lead complex tasks or projects
- Proficiency with systems such as Veeva, RAVE, eCOA, IRT, CTMS
- Strong interpersonal skills with a collaborative, proactive, and adaptable mindset
- Biopharmaceutical industry experience required
Please note PE Global is unable to provide candidates with visa sponsorship. Candidates will need the full right to live and work full time within the UK for at least the next 24 months.
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