Are you ready to drive the future of clinical study? Looking to be in the heart of a company where precision meets purpose?
探花合集 is seeking an experienced and highly organised Clinical Study Specialist to join a global Clinical Operations team supporting the planning, delivery and oversight of clinical studies across Phase I-IV and post-authorisation research programmes.
This role plays a key part in the successful operational delivery of global clinical trials, providing support across study management, site oversight, vendor management, regulatory documentation and cross-functional collaboration. The successful candidate will bring clinical research experience, strong attention to detail and the ability to manage multiple priorities in a fast-paced environment.
Key contract information
Contract type: Freelance contract, Inside IR35
Length: 12-month rolling contract
FTE: full-time
Location: Hybrid in London
Key Responsibilities
Includes, but is not limited to:
- Support the planning, set-up, delivery and close-out of global clinical studies.
- Prepare and maintain study documentation, ensuring accuracy and compliance throughout the study lifecycle.
- Assist with site feasibility, start-up activities, site oversight and issue resolution.
- Coordinate essential study documents, investigator payments and participant tracking activities.
- Support the oversight of CROs and other external vendors, ensuring deliverables are met to agreed timelines and quality standards.
- Maintain Trial Master File (TMF) documentation and support inspection readiness.
- Ensure study activities comply with ICH-GCP, applicable regulations, study protocols and internal procedures.
- Assist with investigator training, study meetings and cross-functional collaboration across Clinical Operations and key stakeholders.
- Support risk identification, mitigation activities and overall study execution.
Candidate Profile
- Degree in Life Sciences, Health Sciences, Nursing, Pharmacy or a related field, or equivalent industry experience.
- Experience supporting clinical trials within a pharmaceutical, biotechnology or CRO environment.
- Experience in oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
- Strong organisational, communication and stakeholder management skills.
- Proactive, detail-oriented and able to manage multiple priorities in a fast-paced environment
If you are having difficulty in applying or if you have any questions, please contact Camille Sandres at c.sandres@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
探花合集 is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 探花合集 is acting as an Employment Agency in relation to this vacancy.
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