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 experienced Clinical Research Physician to join our dynamic clinical trials network in Liverpool. 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 as Principal Investigator (PI) or Sub-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 full GMC registration.
* Minimum 1–2 years of experience in clinical research or clinical trials (preferably Phase II–IV).
* Knowledge of ICH-GCP and 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).