Clinical program lead

EPM Scientific; London; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A leading, innovation-driven biopharmaceutical company seeks a Clinical Program Lead to oversee clinical trials and drive excellence in patient outcomes. This role demands expertise in clinical trial management and collaboration across teams to deliver life-changing therapies. The position offers a hybrid work environment with opportunities for career growth and a strong mission-driven culture.

Benefits

Opportunities for career growth

Flexible hybrid working model

Collaborative, mission-driven culture

Qualifications

• 5+ years of clinical trial management experience in the EU.
• Strong knowledge of ICH/GCP and EU clinical research regulations.
• Experience in pharmaceutical, big pharma, or biotech environments.

Responsibilities

• Lead the planning, execution, and oversight of clinical development programs.
• Serve as the primary point of contact for internal and external stakeholders.
• Ensure compliance with ICH/GCP guidelines and EU regulatory requirements.

Skills

Leadership

Communication

Project Management

Education

Postgraduate qualifications in life sciences, nursing, pharmacy, or medicine

Job description

EPM are collaborating with a leading, innovation-driven biopharmaceutical company is seeking a Clinical program lead to join its expanding clinical development team. This role offers the opportunity to work on cutting-edge therapies for rare and underserved conditions, with a strong focus on clinical excellence and patient outcomes.

About the Role

As Clinical Program Lead, you will be responsible for the strategic and operational leadership of clinical programs from early development through to post-marketing activities. You will work cross-functionally to ensure clinical trials are executed to the highest standards, on time, and within budget. The position requires a hands-on leader with on-site clinical trial experience, capable of managing complex programs and cross-functional teams.

Key Responsibilities

• Lead the planning, execution, and oversight of clinical development programs across multiple indications and geographies.
• Serve as the primary point of contact for internal and external stakeholders, including CROs, investigators, and regulatory bodies.
• Ensure compliance with ICH/GCP guidelines and EU regulatory requirements.
• Collaborate with Medical Affairs, Regulatory, Pharmacovigilance, and Data Management teams.
• Contribute to protocol development, study design, and clinical strategy.
• Oversee clinical trial budgets, timelines, and risk mitigation plans.
• Provide leadership and mentorship to clinical operations staff and project teams.

Requirements

• 5+ years of clinical trial management experience in the EU
• Mandatory experience across all phases of clinical development (Phases I-IV)
• On-site clinical trial experience is essential
• Background in life sciences, nursing, pharmacy, or medicine (postgraduate qualifications desirable)
• Strong knowledge of ICH/GCP and EU clinical research regulations
• Proven experience in pharmaceutical, big pharma, or biotech environments
• Excellent leadership, communication, and project management skills
• Ability to work independently and thrive in a fast-paced, evolving environment

Work Environment

• Hybrid model: 2 days per week in-office, with flexibility for remote work
• Collaborative, mission-driven culture focused on patient outcomes
• Opportunities for career growth and involvement in global clinical strategy

If you're a driven clinical professional with a passion for innovation and excellence, we want to hear from you.
Apply today and become a key player in delivering life-changing therapies to patients who need them most.