🚀 Clinical Protocol Manager

CPL Life Sciences are seeking an experienced Clinical Protocol Manager/Director to provide strategic, scientific, and operational leadership across clinical development programs. This role focuses on driving consistency and quality in protocol development and review, supporting clinical teams to streamline design and execution. The successful individual will work closely with cross-functional teams, governance committees, and senior stakeholders to ensure clinical documents and plans are scientifically robust, aligned with regulatory expectations, and developed efficiently. This role is an initial 12 month contract with scope of extension, inside IR35 offering up to £550-£570 per day. The position is a hybrid role based in central London, ideally 2 days per week on site a week. Key Experience & Skills: Strong expertise in clinical protocol development and review Experience with Clinical Development Plans (CDPs) Familiarity with scientific review committees or governance bodies Proven ability to lead cross-functional collaboration Background in regulatory document preparation (e.g., DMC charters) Strategic thinking and operational planning skills Experience in clinical trial design and methodology Strong communication and stakeholder management skills Ability to drive process improvement initiatives Understanding of digital tools in clinical trial execution 12 month contract London - Hybrid £570 per day (Umbrella)