Clinical Project Manager - Site Initiation

Coronado Research; Greater London; On-site; GBP 60,000 - 80,000; Full time

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

We are urgently seeking a Clinical Project Manager who is able to work on-site in Central London with expertise in study start up, site contract negotiation as well as clinical project management.

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.

Responsibilities

• 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.

Qualifications

• 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.