At a Glance
- Tasks: Lead and manage EU clinical trial programs from design to reporting.
- Company: Global specialty pharmaceutical group focused on innovative treatments.
- Benefits: Competitive salary, hybrid working model, and professional development opportunities.
- Other info: Dynamic role with high visibility and ownership in a growing global organisation.
- Why this job: Make a real difference in patients' lives while working with leading scientific experts.
- Qualifications: Graduate degree in relevant field and experience in managing EU clinical trials.
The predicted salary is between 60000 - 75000 € per year.
Surrey, United Kingdom | Hybrid (2-3 days onsite) | Permanent, Full‑Time
We are looking for a Clinical Program Lead for a global specialty pharmaceutical group dedicated to developing and commercialising innovative treatments for patients with genetic, metabolic, systemic, and life‑threatening conditions, to join the Global Clinical Affairs team and lead the delivery of EU clinical trial programs.
Key Responsibilities
- Clinical Program Delivery
- Lead end‑to‑end EU clinical programs from design through reporting
- Implement clinical program strategy and contribute to overall Clinical Affairs objectives
- Maintain holistic oversight of timelines, risks, quality, and budgets
- Proactively communicate progress, risks, and issues to senior leadership
- Drive cross‑functional alignment and knowledge sharing
- Study Execution & Oversight
- Lead protocol development, applying Quality by Design principles
- Oversee study monitoring, ensuring data quality, integrity, and participant safety
- Supervise data management activities including cleaning and review
- Review analyses and lead Clinical Study Report (CSR) development
- Ensure inspection readiness and support GCP audits and regulatory inspections
- Sites, Vendors & External Partners
- Oversee site selection, contracts, budgets, recruitment, and performance
- Manage relationships with investigators, expert physicians, and key opinion leaders
- Lead investigator meetings, site initiation, and accreditation activities
- Select and oversee CROs and service providers, ensuring performance against scope and quality expectations
- Leadership & People Management
- Lead, coach, and mentor members of the Clinical Operations team
- Manage direct reports and support professional development initiatives
- Oversee resource planning and workload allocation within the program
- Support internal training and capability building
- Program Enablement & Innovation
- Contribute to clinical process improvement and trial modernisation initiatives
- Support digital integration and operational efficiency across the portfolio
- Represent the company at conferences, external events, and regulatory meetings as required
Essential Requirements
- Graduate degree in Biological Sciences, Nursing, Pharmacy, or Medicine (postgraduate qualification desirable)
- Strong working knowledge of EU clinical trial regulations and ICH‑GCP
- Proven experience managing EU clinical trials and clinical programs
- Experience overseeing data management and clinical reporting
- Demonstrated leadership and team management capability
- Strong project management, communication, and stakeholder engagement skills
- Ability to work independently and manage complex programs to tight timelines
What's on Offer
- Competitive salary and benefits package
- Opportunity to work alongside world‑leading scientific experts
- High level of ownership and visibility within a growing global organisation
- Hands‑on role contributing directly to therapies that improve patients' lives
- Hybrid working model with flexibility
Desired Skills and Experience
- Clinical Leadership & Strategy
- Clinical Program Leadership
- EU Clinical Trial Strategy
- End‑to‑End Clinical Program Delivery
- Portfolio Oversight
- Clinical Development Planning
- Quality by Design (QbD)
- Clinical Affairs Strategy
- Cross‑Functional Leadership
- Risk Assessment & Mitigation
- Governance & Decision Making
- Clinical Operations & Study Execution
- Interventional Clinical Trials
- Non‑Interventional / Observational Studies
- EU Clinical Trial Management
- Study Start‑Up to Close‑Out
- Site Selection & Feasibility
- Investigator Management
- Site Initiation & Accreditation
- Recruitment Strategy & Oversight
- Protocol Development
- Study Monitoring Oversight
- Vendor Oversight (CROs, Service Providers)
- Regulatory, Compliance & Quality
- ICH‑GCP Compliance
- EU Clinical Trial Regulations
- Inspection Readiness
- GCP Audits & Inspections
- Ethics Committee Submissions
- Competent Authority Submissions
- SOP Development & Adherence
- Trial Master File (TMF) Oversight
- Records Management
- Participant Safety & Data Integrity
- Data, Reporting & Scientific Excellence
- Clinical Data Management Oversight
- Data Cleaning & Validation
- Data Integrity & Quality Control
- Clinical Data Review & Interpretation
- Statistical Review Collaboration
- Clinical Study Reports (CSRs)
- Scientific Literature Review
- Medical & Scientific Writing
- Benefit‑Risk Evaluation
- Stakeholder & External Engagement
- Principal Investigator Relationships
- Key Opinion Leader (KOL) Engagement
- Investigator Meetings
- Regulatory Authority Meetings
- Conference Representation
- External Communications Support
- People & Resource Management
- Line Management
- Team Leadership & Mentoring
- Performance Coaching
- Resource Planning
- Workforce Allocation
- Training & Capability Building
- Professional Development Support
- Process Improvement & Innovation
- Clinical Process Optimisation
- Trial Modernisation
- Digital & Technology Integration
- Operational Efficiency Initiatives
Clinical Program Lead in London employer: EPM Scientific
Join a global specialty pharmaceutical group in Surrey, where you will lead innovative clinical programs that directly impact patient lives. With a competitive salary and benefits package, a hybrid working model, and opportunities for professional development, this role offers a unique chance to work alongside world-leading experts in a supportive and dynamic environment. Embrace the high level of ownership and visibility within a growing organisation dedicated to improving health outcomes through cutting-edge therapies.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Program Lead in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical field, attend industry events, and engage on platforms like LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Be ready to discuss how your experience aligns with their goals, especially in EU clinical trials. Show them you’re not just another candidate, but someone who truly understands their mission.
✨Tip Number 3
Practice your pitch! You want to be able to clearly articulate your experience and how it relates to the Clinical Program Lead role. Keep it concise and impactful – think of it as your personal brand statement.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take that extra step to connect directly with us.
We think you need these skills to ace Clinical Program Lead in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Program Lead role. Highlight your experience with EU clinical trials and any leadership roles you've held. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical program management and how you can contribute to our mission. Keep it engaging and relevant to the job description.
Showcase Your Achievements:When detailing your experience, focus on specific achievements rather than just duties. Use metrics where possible to demonstrate your impact in previous roles. We love seeing how you've made a difference!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at EPM Scientific
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your knowledge of EU clinical trial regulations and ICH-GCP. Be ready to discuss your previous experiences managing clinical trials, focusing on specific challenges you faced and how you overcame them.
✨Showcase Your Leadership Skills
As a Clinical Program Lead, you'll need to demonstrate strong leadership capabilities. Prepare examples of how you've led teams, mentored colleagues, and managed cross-functional projects. Highlight your ability to drive alignment and foster collaboration.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills. Think about potential risks in clinical programs and how you would mitigate them. Practising these scenarios can help you articulate your thought process clearly during the interview.
✨Communicate Your Vision for Innovation
The role involves contributing to clinical process improvement and trial modernisation. Be prepared to share your ideas on how to enhance operational efficiency and integrate digital solutions into clinical programs. This shows you're forward-thinking and aligned with the company's goals.
