Clinical Project Manager (Contractor)

Ergomed; Guildford; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading mid-sized CRO is seeking a contract Project Manager with extensive experience managing global trials in oncology. In this pivotal role, you will ensure project delivery meets quality standards while coordinating with cross-functional teams. The ideal candidate will possess strong analytical and communication skills and hold a Bachelor's Degree in a related field, offering the opportunity to make a significant impact on patient care.

Qualifications

• Experience managing international clinical trials within a CRO environment.
• Extensive experience with global trials in radiopharmaceuticals, gastrointestinal, lung, or breast cancers.
• Bid defense experience.

Responsibilities

• Ensure projects are delivered on time, within budget, and within scope.
• Coordinate with project team members, providing training as needed.
• Develop and update project plans to align with goals.

Skills

Analytical skills

Organizational skills

Communication skills

Education

Bachelor’s Degree in a science-related discipline

Job description

Company Description

Ergomed Group is a rapidly expanding full-service mid-sized CRO specialising in Oncology and Rare Disease.

Since its foundation in 1997, the company has grown organically and steadily through strategic investments and landmark acquisitions, with operations in Europe, North America, and Asia.

We have fostered a truly international culture at Ergomed.

Join us on this exciting journey to make a positive impact on patients' lives.

Job Description

We are recruiting a contract Project Manager with extensive experience managing global trials in one of the following indications:

• Radiopharmaceuticals
• Gastrointestinal cancer
• Lung cancer
• Breast cancer

Responsibilities:

• Ensure projects are delivered on time, within budget, and within scope, maintaining industry, sponsor, and Ergomed quality standards.
• Coordinate with project team members, provide training as needed, and ensure proper task allocation.
• Develop, review, and update project plans to align with goals and milestones.
• Organize and facilitate study-related meetings (initiation, execution, closure).

• Serve as the main contact with sponsors and Ergomed Senior Management regarding project status.
• Represent Ergomed at external meetings, liaising with scientific/medical experts and participating in committee meetings (e.g., EC/IRB).
• Review and develop SOPs to ensure regulatory compliance and create training programs supporting study activities.
• Contribute to bid defense activities.

Qualifications

• Experience managing international clinical trials within a CRO environment.

• Extensive experience with global trials in radiopharmaceuticals, gastrointestinal, lung, or breast cancers.
• Bid defense experience.
• Strong analytical, organizational, and communication skills.
• Bachelor’s Degree in a science-related discipline.

Additional Information

Our core values are integral to our operations. If they resonate with you, Ergomed is an excellent company to join!

Quality

Integrity & Trust

Drive & Passion

Agility & Responsiveness

Belonging

Collaborative Partnerships

We look forward to receiving your application.