Clinical Research Physician – (Sub-Investigator) – UK Growing UK Site Network

Greenlsr; Peterborough; On-site; GBP 100,000 - 125,000; Full time

Job summary

A leading recruitment firm is offering an exciting position for a Clinical Research Physician as a Sub-Investigator. This role requires a GMC-registered physician who will collaborate with Principal Investigators and multidisciplinary teams to ensure compliance with clinical trial standards. Strong communication and teamwork skills are essential, along with a keen interest in clinical trials. This is an on-site position located in Peterborough, Nottingham, Brighton, or Birmingham.

Qualifications

• GMC-registered physician (Full registration, license to practice).
• Prior experience in clinical research is advantageous but not essential.
• Strong interest in clinical trials, patient care, and evidence-based medicine.

Responsibilities

• Conduct clinical trial activities as a Sub-Investigator under supervision.
• Perform study assessments and ensure participant safety.
• Collaborate to ensure adherence to study protocols and regulations.

Skills

Excellent communication skills

Teamwork

Interest in clinical trials

Education

GMC registration

Job description

Clinical Research Physician – United Kingdom

Job Title: Clinical Research Physician (Sub-Investigator)

Location: Peterborough, Nottingham, Brighton, or Birmingham (On-site)

About The Role:

We’re looking for an enthusiastic and dedicated Clinical Research Physician to join our growing UK site network as a Sub-Investigator. This is an excellent opportunity for doctors interested in clinical research to play a key role in the delivery of early and late-phase clinical trials across a range of therapeutic areas.

You’ll work alongside experienced Principal Investigators and multidisciplinary teams to ensure the highest standards of patient care, data quality, and regulatory compliance.

Key Responsibilities:

• Conduct clinical trial activities as a Sub-Investigator under the supervision of the Principal Investigator.
• Perform study assessments, review medical histories, and ensure participant safety and well-being.
• Collaborate with site staff to ensure adherence to study protocols, GCP, and regulatory requirements.
• Contribute to ongoing study feasibility, recruitment, and retention efforts.
• Maintain accurate and timely documentation within the trial master file and electronic data capture systems.

About You:

• GMC-registered physician (Full registration, license to practise).
• Prior experience in clinical research is advantageous but not essential – full training will be provided.
• Strong interest in clinical trials, patient care, and evidence-based medicine.
• Excellent communication and teamwork skills.
• Ability to work on-site in one of our UK research centres: Peterborough, Nottingham, Brighton, or Birmingham.

How To Apply

• Email your CV and cover letter to [e-mail]
• View more roles at Green Life Science Recruitment
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