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Project Manager - Clinical Operations
Location: Remote UK
About the Role
Novotech is seeking an experienced Project Manager to lead the successful delivery of global clinical trials from study start-up through close-out. As the primary point of contact for sponsors, you will oversee project planning, execution, financial management, and cross-functional collaboration to ensure studies are delivered on time, within budget, and in compliance with ICH-GCP, applicable regulations, and Novotech SOPs.
This role requires a proactive leader with strong stakeholder management skills, commercial awareness, and the ability to manage multiple priorities while driving operational excellence.
Key Responsibilities
Project Leadership
- Lead the end-to-end delivery of clinical studies from feasibility and site selection through study close-out.
- Develop and maintain project plans, timelines, risk registers, and study tracking tools.
- Coordinate cross-functional teams, including Clinical Operations, Regulatory Affairs, Biometrics, Medical, Pharmacovigilance, and Vendor Management.
- Identify project risks and implement mitigation strategies to ensure successful study delivery.
- Ensure projects are conducted in accordance with study protocols, ICH-GCP, local regulations, and company SOPs.
Client & Stakeholder Management
- Serve as the primary point of contact for sponsors throughout the project lifecycle.
- Build strong client relationships through regular communication, project updates, and proactive issue resolution.
- Lead project meetings, governance calls, and contribute to bid defence meetings where required.
- Collaborate with Business Development during feasibility assessments and change order activities.
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Financial & Operational Management
- Manage project budgets, revenue forecasts, profitability, and financial performance.
- Monitor project scope and coordinate change orders as required.
- Ensure appropriate project resourcing and support effective workload planning.
- Oversee vendor selection and management to ensure quality delivery.
Site & Study Management
- Oversee site selection, activation, recruitment, monitoring, and study close-out activities.
- Support ethics and regulatory submissions in collaboration with Clinical Operations and Regulatory teams.
- Monitor recruitment performance and implement strategies to improve enrolment and site performance.
- Ensure inspection and audit readiness throughout the study lifecycle.
Leadership & Continuous Improvement
- Lead, mentor, and support cross-functional project teams, including Associate Project Managers.
- Foster collaboration, accountability, and high-performance project execution.
- Contribute to process improvements, SOP development, and operational excellence initiatives.
- Represent Novotech professionally with sponsors, investigators, and industry stakeholders.
About You
You are an experienced clinical project leader with excellent organisational, leadership, and communication skills. You thrive in a fast-paced, collaborative environment and are passionate about delivering high-quality clinical research while building strong client relationships.
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Qualifications & Experience
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biomedical Sciences, or a related discipline.
- Significant experience in clinical project management within a CRO, pharmaceutical, or biotechnology environment.
- Strong understanding of the clinical trial lifecycle, including study start-up, site management, recruitment, data management, and study close-out.
- Comprehensive knowledge of ICH-GCP, global clinical trial regulations, and sponsor requirements.
- Proven experience managing cross-functional global clinical teams, budgets, timelines, and project risks.
- Strong client-facing experience with the ability to build trusted sponsor relationships.
- Experience with CTMS, eTMF, Microsoft Office, and other clinical trial management systems.
- Excellent communication, negotiation, and stakeholder management skills.
Why Join Novotech?
At Novotech, you'll join a global CRO known for delivering high-quality clinical research across the Asia-Pacific region, North America, and Europe. We offer a collaborative culture, opportunities for career growth, and the chance to contribute to innovative clinical trials that improve patient outcomes worldwide.
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