Clinical Research Physician (North East England)
Key Responsibilities
- Act as Principal Investigator or Sub-Investigator across a portfolio of clinical trials.
- Conduct medical assessments and ensure participant safety throughout study participation.
- Review eligibility criteria, medical histories, laboratory data, and adverse events.
- Support study feasibility, start-up activities, and sponsor engagement.
- Ensure all studies are conducted in accordance with ICH-GCP, protocol requirements, and regulatory standards.
- Provide medical oversight to research nurses, coordinators, and site staff.
- Participate in sponsor meetings, monitoring visits, and audits.
- Contribute to the continued growth and clinical excellence of the organisation.
Candidate Profile
We welcome applications from physicians with experience in one or more of the following areas:
- Endocrinology & Diabetes
- Cardiometabolic Medicine
- Neuroscience
- Neurology
- Pain Medicine
- Internal Medicine
- Clinical Pharmacology
Requirements
- GMC-registered Physician.
- Previous clinical trial experience as a PI, Sub-Investigator, or treating physician highly desirable.
- Strong understanding of clinical research and GCP principles.
- Excellent communication and stakeholder management skills.
- Ability to work within a fast-paced commercial research environment.
- Passion for clinical innovation and improving patient access to novel therapies.
What's on Offer?
- Opportunity to work on innovative clinical trials sponsored by leading global pharmaceutical and biotech companies.
- Exposure to a broad range of therapeutic areas, including CNS, Pain, Metabolic Disease, and Endocrinology.
- Career development towards Principal Investigator, Medical Director, or Clinical Development pathways.
- Collaborative and entrepreneurial environment within a growing research organisation.
- Competitive salary, benefits, and ongoing professional development support.
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