Contract Project Manager - Radiopharmaceuticals, Gastro / Lung / Breast Cancer, Duchenne Muscul[...]

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

Job summary

A leading company in clinical research is seeking a Project Manager or Clinical Team Manager to oversee global trials in oncology and rare diseases. The ideal candidate will have experience in managing complex clinical trials and a strong background in science. Join a dynamic team dedicated to improving patient outcomes and ensuring project success through quality and integrity.

Qualifications

• Experience as a Project Manager of international clinical trials in a CRO environment.
• Experience with global Radiopharmaceuticals, Gastrointestinal / Lung / Breast Cancer, or Duchenne Muscular Dystrophy clinical trials.

Responsibilities

• Ensure projects are delivered on time, within budget, and scope.
• Liaise with project team members and provide training.
• Serve as the primary contact with sponsors regarding project status.

Skills

Analytical

Organizational

Communication

Education

Bachelor’s Degree in a science-related discipline

Job description

Company Description

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

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 true international culture here at Ergomed.

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

Job Description

We are recruiting for a contract Project Manager or contract Clinical Team Manager with previous experience managing global trials in Radiopharmaceuticals, Gastrointestinal / Lung / Breast Cancer, or Duchenne Muscular Dystrophy.

• Ensure that projects are delivered on time, within budget, and within scope, maintaining industry, sponsor, and Ergomed quality standards.
• Liaise with project team members, provide training where needed, and ensure correct task allocation.
• Develop, review, and edit project plans to align with goals and milestones.
• Organize and facilitate project meetings related to study activities (study organization, initiation, execution, closure).

• Serve as the primary contact with sponsors and Ergomed Senior Management regarding project status.
• Represent Ergomed at external meetings, liaising with scientific/medical experts in other CROs/Sponsors and for committee meetings (e.g., EC/IRB).
• Review and edit relevant SOPs to ensure compliance with regulatory standards and develop study-related training programs.
• Contribute to bid defense activities.

Qualifications

• Experience as a Project Manager of international clinical trials in a CRO environment.
• Experience with global Radiopharmaceuticals, Gastrointestinal / Lung / Breast Cancer, or Duchenne Muscular Dystrophy clinical trials.
• Strong analytical, organizational, and communication skills.
• Bachelor’s Degree in a science-related discipline.

Additional Information

Our core values are central to our operations. If these resonate with you, Ergomed is a great company to join!

• Quality
• Integrity & Trust
• Drive & Passion
• Agility & Responsiveness
• Belonging
• Collaborative Partnerships

We look forward to receiving your application.