Your resume and cover letter, tailored to exactly what they’re hiring for.
Get past ATS filters
Job summary
A global clinical research organization is urgently seeking a Clinical Project Manager to work on-site in central London. The ideal candidate will have 5-10 years of clinical project management experience, particularly in cardiovascular studies, and strong regulatory affairs expertise. Responsibilities include managing study operations, ensuring compliance with ICH-GCP, and supporting the clinical operations team. This position offers a unique opportunity to contribute to impactful clinical trials across multiple therapeutic areas.
Qualifications
5-10 years of overall clinical project management experience required.
Experience managing timelines and multi-site studies crucial.
Solid experience in regulatory affairs, especially submissions.
Responsibilities
Provide short-term project management support for ongoing studies.
Oversee study operations, vendors, and external partners.
Support team coordination and preparation of study materials.
Skills
Clinical project management
Regulatory affairs
Communication skills
Problem-solving skills
Organizational skills
Job description
A global clinical research organization is urgently seeking a Clinical Project Manager to work on-site in central London. The ideal candidate will have 5-10 years of clinical project management experience, particularly in cardiovascular studies, and strong regulatory affairs expertise. Responsibilities include managing study operations, ensuring compliance with ICH-GCP, and supporting the clinical operations team. This position offers a unique opportunity to contribute to impactful clinical trials across multiple therapeutic areas.