At a Glance
- Tasks: Drive the future of clinical studies and support global trials from planning to delivery.
- Company: Join Proclinical, a leader in clinical operations with a purpose-driven culture.
- Benefits: Freelance contract, hybrid work in London, and opportunities for professional growth.
- Other info: Fast-paced environment with a focus on collaboration and career development.
- Why this job: Make a real impact in healthcare by managing innovative clinical research projects.
- Qualifications: Degree in Life Sciences or related field and experience in clinical trials.
The predicted salary is between 40000 - 55000 £ per year.
Are you ready to drive the future of clinical study? Looking to be in the heart of a company where precision meets purpose? Proclinical 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
- 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.
Study Specialist II employer: Proclinical Group
Proclinical is an exceptional employer that fosters a dynamic and collaborative work environment, ideal for those passionate about advancing clinical research. With a strong focus on employee growth, we offer comprehensive training and development opportunities, ensuring our team members thrive in their careers while contributing to impactful global studies. Located in the vibrant city of London, our hybrid work model promotes a healthy work-life balance, making Proclinical a rewarding place to build your future.
