Hobson Prior

About the Company

Hobson Prior is a leading specialist life sciences recruiter focused on finding and placing outstanding candidates across Europe, the US and Asia Pacific.

We've placed over 6000 senior-to-mid level life sciences professionals across 25 countries. With a large network of clients and candidates, we aim to build recruitment relationships so we can match the top talent with the best projects and often exclusive opportunities, in line with your career aspirations.

Listed Jobs

Company Name

Hobson Prior

Job Title

Study Coordinator // UK based

Job Description

**Job Title** Study Coordinator (UK) **Role Summary** Part‑time, freelance Study Coordinator responsible for managing patient‑level activities within clinical research studies. Acts as the primary liaison between patients, investigators and study teams, ensuring adherence to protocols, data integrity and regulatory compliance. **Expectations** * Maintain accurate study documentation and timely data entry. * Guide patients through the informed consent process. * Coordinate assessments, logistics and communication across sites. * Monitor and report adverse events (AEs/SAEs). * Perform quality checks and support query resolution. * Ensure inspection readiness and compliance with training requirements. * Manage daily tasks, prioritize workload and propose solutions to complex issues. **Key Responsibilities** 1. Conduct patient informed consent and record compliance. 2. Schedule and track study assessments. 3. Enter and verify data in electronic systems. 4. Coordinate patient, investigator and study‑site activities. 5. Report AEs/SAEs to the study team. 6. Perform data quality checks and resolve queries. 7. Build and maintain relationships with patients, investigators and research teams. 8. Manage travel (≤10%) and travel documents. 9. Support site activation and ongoing monitoring. **Required Skills** * Native‑level English proficiency. * Strong organizational, communication and time‑management skills. * Knowledge of clinical research processes, GCP, and patient safety reporting. * Ability to navigate clinical technologies and troubleshoot issues. * Professionalism, problem‑solving and escalation handling. * Understanding of data collection best practices to minimise queries. **Required Education & Certifications** * Relevant post‑secondary education or equivalent experience in clinical research, medical or related field. * Familiarity with Good Clinical Practice (GCP) guidelines. *Right to work in the UK required.*

London, United kingdom

On site

18-09-2025