Clinical Research Physician

Job Title:Clinical Research Physician

Location:Liverpool, UK

Employment Type:Full-time

Reports To:Medical Director / Principal Investigator / Site Director

About the Role:

We are seeking a motivated and experiencedClinical Research Physicianto join our dynamic clinical trials network inLiverpool. This is a patient-facing role where you will act as a Sub-Investigator or Principal Investigator across a range of Phase I–IV clinical studies in collaboration with global sponsors and CROs. You will play a pivotal role in delivering high-quality clinical research within a network of well-established trial sites.

Key Responsibilities:

• Serve asPrincipal Investigator (PI)orSub-Investigator (Sub-I)on assigned clinical trials.
• Provide medical oversight and ensure participant safety throughout the study lifecycle.
• Conduct study-related procedures including medical assessments, physical examinations, and AE/SAE evaluations.
• Review and assess eligibility criteria, informed consent documentation, and patient medical histories.
• Liaise with study sponsors, monitors (CRAs), ethics committees, and regulatory authorities as needed.
• Ensure GCP compliance and adherence to protocol, SOPs, and applicable regulations.
• Contribute to site feasibility, study start-up, and recruitment planning activities.
• Support medical input into recruitment materials and protocol reviews.
• Maintain accurate documentation in accordance with regulatory and sponsor expectations.
• Provide clinical leadership and guidance to site staff including nurses, coordinators, and administrative teams.

Essential Qualifications and Experience:

• Medical degree (MBBS, MBChB or equivalent) and fullGMC registration.
• Minimum 1–2 years of experience inclinical researchor clinical trials (preferably Phase II–IV).
• Knowledge ofICH-GCPand UK clinical trial regulations.
• Excellent clinical judgment and ability to make sound medical decisions.
• Strong communication and interpersonal skills.
• Ability to work effectively within a multidisciplinary team.

Desirable:

• Experience acting as PI or Sub-I in commercial clinical trials.
• Background in general medicine, internal medicine, or a therapeutic area relevant to trials (e.g., vaccines, cardiology, respiratory, CNS).
• Interest in expanding research expertise and participating in multiple therapeutic areas.
• ALS/BLS certification (training can be provided).