Job Title : Director, Clinical Processes & Solutions
📍 Location : London, UK (Hybrid or Remote)
📅 Contract Length : 12–18 months
💼 Pay Rate : £600 / day via Umbrella only
Job Purpose
- We are seeking an experienced Director, Clinical Processes & Solutions to lead and drive cross-functional clinical development (CD) processes and initiatives across global teams. This is a pivotal leadership role that ensures the development, implementation, and continuous improvement of end-to-end clinical processes, maintaining alignment with global regulatory standards and inspection readiness.
- This role will collaborate extensively with Process, Risk & Surveillance (PRS), Clinical Development, Global Clinical Operations, Regulatory Affairs, and Quality Assurance teams to drive operational excellence and regulatory compliance across Development Units and Global Line Functions.
Key Responsibilities
Lead cross-functional alignment of clinical development processes and oversee their implementation across Development Units.Ensure clinical processes meet regulatory requirements and are audit / inspection-ready, working in partnership with QA, PRS, and other key stakeholders.Represent CD processes in Health Authority inspections and internal / external audits.Establish and maintain a global network of Subject Matter Experts (SMEs) to support inspection readiness and process improvement.Continuously enhance clinical processes using performance metrics, root cause analysis, and new technologies.Author and maintain SOPs, working practices, guidance documents, and key clinical templates.Drive best practice adoption through training, process guidance, and operational support for cross-functional teams.Lead or contribute to strategic CD initiatives and projects that have broad business impact.Coordinate QA / SOP-related activities, including SME engagement and document reviews.Act as a key advisor to CD Leadership, ensuring timely communication and issue escalation.Provide leadership continuity by deputizing for senior leaders in Business Solutions and Clinical Compliance as needed.Ideal Candidate Profile
Education & Language Requirements :Advanced degree in life sciences or a clinically relevant field (e.g., MSc, PharmD, PhD preferred)Fluent in English (written and spoken)Experience & Skills :
10+ years of technical and operational experience in planning and managing clinical studies within pharma or academiaIn-depth knowledge of pharmaceutical development, GCP, regulatory requirements, and quality systemsDemonstrated expertise in designing and implementing efficient, compliant end-to-end clinical processesStrong project and stakeholder management skills, with the ability to lead cross-functional global teamsProven leadership capabilities, including coaching, influence without authority, and navigating complex organizationsExcellent interpersonal, communication, and negotiation skillsComfortable working independently and taking accountability in high-impact environmentsAction-oriented with a track record of driving change and delivering resultsExperience representing clinical functions during audits and inspectionsImpact & Scope
Matrix leadership of global teams across clinical development and related functionsAccountability for third-party spend related to process development and document supportDirect impact on the quality and efficiency of global clinical development programsReady to lead global clinical excellence and drive meaningful change in clinical development processes? Apply now to be considered for this strategic leadership opportunity.