Job Title: Vice President of Clinical Operations
Location: United Kingdom (Hybrid or On-site)
Industry: Biotechnology / Oncology
Reports to: Chief Medical Officer or Chief Executive Officer
About Us
We are a pioneering biotechnology company focused on oncology. Our goal is to develop breakthrough therapies that meet critical needs in cancer treatment. We are driven by our mission: to improve patient outcomes by advancing new, targeted treatments through clinical development and regulatory approval.
About the Role
We are looking for a Vice President of Clinical Operations to lead our clinical trials and drive our operational strategy. This is a senior leadership role with a direct impact on our development pipeline and future commercial success.
You will be responsible for managing all aspects of clinical operations—from planning and execution to closing trials. This role is ideal for someone with strong strategic vision, leadership skills, and experience in global oncology trials.
Key Responsibilities
1. Strategic Leadership
-
Define and execute our clinical operations strategy.
-
Align operations with corporate goals and regulatory standards.
2. Clinical Trial Oversight
-
Lead clinical trials from Phase I to III.
-
Ensure trials meet GCP/ICH guidelines, timelines, and quality standards.
3. Team Leadership
-
Build and lead a high-performing clinical team.
-
Support employee growth and foster a culture of accountability and innovation.
4. Vendor and CRO Management
-
Select and manage external partners such as CROs and labs.
-
Ensure high-quality work and stay on budget.
5. Budget and Resources
-
Manage budgets, timelines, and resource planning.
-
Optimize operations across all studies.
6. Cross-functional Collaboration
-
Work closely with departments like Clinical Development, Regulatory, Medical Affairs, Biostatistics, and Data Management.
-
Align on development plans and trial execution.
7. Regulatory Compliance
-
Ensure all trials follow global regulations and internal procedures.
-
Maintain ethical standards across operations.
8. Continuous Improvement
-
Improve systems, processes, and tools for scalability and efficiency.
Qualifications
-
Advanced degree (PhD, PharmD, MD, or MSc) in life sciences or a related field.
-
Experience in oncology is essential.
-
15+ years in clinical operations within biotech/pharma, including 5+ years in a senior role.
-
Proven success managing global oncology trials from early to late phase.
-
Strong knowledge of ICH-GCP and EMA/MHRA regulations.
-
Experience with regulatory submissions (CTA, IND, NDA/MAA).
-
Excellent leadership, communication, and strategic thinking skills.
-
Ability to perform well in a fast-paced, evolving environment.
What We Offer
-
A key leadership role in an innovative biotech company.
-
A chance to shape the future of cancer treatment.
-
Competitive salary with equity options.
-
A collaborative, mission-driven culture.
-
Flexible work setup (hybrid or on-site).
If you’re passionate about making a difference in oncology and have the experience to lead global clinical trials, we want to hear from you.