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.