Lead Clinical Trials Physician (PI/Sub-PI) UK

EPM Scientific; Greater London; On-site; GBP 90,000 - 130,000; Full time

Job summary

EPM Scientific is seeking experienced physicians to join its clinical development team in the UK, offering Sub-Investigator (Sub-PI) or Principal Investigator (PI) roles across multiple therapeutic areas and trial phases.

These positions focus on high-quality patient safety, regulatory compliance, and data integrity, with opportunities to lead site activities, mentor study staff, and collaborate with sponsors and CRO partners in a fast-paced, global environment.

Qualifications

• Medical degree and GMC registration with fitness to practice.
• Experience in clinical trials across phases I–IV preferred.
• Experience as Sub-Investigator or PI highly desirable.

Responsibilities

• Conduct and oversee clinical trial activities in accordance with GCP, protocol requirements, and regulatory standards.
• Perform medical assessments, physical examinations, and safety evaluations of study participants.
• Support participant recruitment, screening, enrollment, and ongoing trial management.
• Review safety information, adverse events, and clinical data throughout study conduct.
• Collaborate closely with clinical operations, sponsors, research nurses, and site staff.
• Contribute to investigator meetings, protocol training, and study-related documentation.
• Ensure high standards of participant safety, data integrity, and regulatory compliance.

Skills

Clinical Research

Clinical Trials

GCP

Stakeholder Management

Multidisciplinary Collaboration

Communication Skills

Education

Medical degree (MBBS/MBChB/MD) or equivalent

GMC Registration

Job description

EPM Scientific is seeking experienced physicians to join its clinical development team in the UK, offering Sub-Investigator (Sub-PI) or Principal Investigator (PI) roles across multiple therapeutic areas and trial phases.

These positions focus on high-quality patient safety, regulatory compliance, and data integrity, with opportunities to lead site activities, mentor study staff, and collaborate with sponsors and CRO partners in a fast-paced, global environment.