EPM Scientific
Clinical Program Leader
Surrey
€80k – €100k/yr
Posted about 12 hours ago
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Key Responsibilities
Clinical Program Leadership
- Lead global and European clinical programs across a rare disease portfolio from planning through execution and study completion.
- Drive program delivery, ensuring alignment with broader clinical development and corporate objectives.
- Maintain oversight of timelines, budgets, quality metrics, risk management, and overall program performance.
- Provide regular strategic updates and recommendations to senior leadership and governance committees.
- Coordinate and lead cross-functional teams across Clinical Operations, Medical Affairs, Regulatory Affairs, Biometrics, Drug Safety, and external partners.
- Support the progression of rare disease indications through key development milestones and toward approval.
Clinical Execution & Delivery
- Ensure operational excellence across all stages of clinical trial delivery.
- Provide oversight of study conduct, patient safety, data integrity, and regulatory compliance.
- Support protocol development and implementation of Quality by Design principles.
- Review clinical data, study progress, and key performance indicators to drive informed decision-making.
- Lead study reporting activities, CSR development, and support regulatory submissions.
- Maintain inspection readiness and oversee audit preparation and regulatory interactions.
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Cross-Functional Leadership
- Lead multidisciplinary project teams to deliver program objectives efficiently and effectively.
- Foster strong collaboration between internal functions and external stakeholders.
- Drive accountability and alignment across all program contributors.
- Act as a key clinical representative during governance meetings and strategic planning discussions.
- Build strong working relationships with investigators, KOLs, CROs, and vendors.
Site & Vendor Oversight
- Oversee site feasibility, site selection, contracting, budgets, recruitment, and operational performance.
- Lead vendor selection, governance, and performance management activities.
- Ensure CROs and service providers deliver against agreed timelines and quality expectations.
- Support investigator engagement, site training initiatives, and study-related meetings.
- Provide guidance and oversight to Clinical Study Leads and Clinical Project Associates.
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Leadership & Team Development
- Provide leadership, coaching, and mentorship across clinical teams.
- Support resource planning and allocation across programs.
- Develop team capabilities through training, knowledge sharing, and best practice initiatives.
- Foster a culture of continuous improvement, collaboration, and operational excellence.
- Contribute to the ongoing growth and development of the Clinical Affairs function.
Innovation & Continuous Improvement
- Identify opportunities to enhance clinical trial execution and program efficiency.
- Support implementation of innovative approaches, technologies, and digital solutions.
- Drive process improvements across the clinical development organisation.
- Contribute to external scientific and clinical communications where appropriate.
- Represent the organisation at industry meetings, conferences, and regulatory interactions.
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Skills
Clinical Program Leadership
Clinical Trial Execution
Cross-functional Leadership
Vendor Management
Risk Management
Budget Oversight
Regulatory Compliance
Protocol Development
CSR Development
Site Feasibility
Stakeholder Management
Resource Planning
Quality by Design
Patient Safety
Data Integrity
Mentorship
Location