Our client has an extensive global network of sites they work with to provide clinical trials to a range of sponsors and across various Therapeutic areas, although there is a focus on cardiovascular, haematology and oncology therapeutic areas.

Ideally, we are seeking a CMP with a minimum of three years' experience in the role - someone who can quickly adapt and provide effective support to the team in the background. Strong regulatory affairs experience (e.g., submissions) is essential.

Scope of Work

• Provide short-term project management support to an ongoing clinical study, ensuring delivery within agreed timelines, budgets, and quality standards, in full compliance with ICH-GCP, SOPs, and regulatory requirements.
• Oversee study operations and vendors, including CROs, sites, and external partners, maintaining effective communication, risk management, and documentation (e.g., TMF, contracts, budgets, and reports).
• Support the Clinical Operations team with coordination, issue resolution, and preparation of key study materials, contributing to process improvement and ensuring continuity during team absences.

Essential Experience:

• 5-10 years of overall clinical project management experience within a CRO or sponsor environment.
• Proven ability to manage timelines, vendors, and multi-site studies in accordance with ICH-GCP.
• Strong communication, organizational, and problem-solving skills; experience in cardiovascular studies preferred.
• Solid experience in regulatory affairs (submissions and documentation).
• Global experience managing complex interventional and observational studies.

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