Clinical Project Manager (Contractor)

Ergomed; Paris; Sur place; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A leading full-service CRO is seeking a skilled Project Manager to oversee global trials focusing on radiopharmaceuticals and various cancers. The role involves ensuring project delivery within set standards and timelines while engaging with sponsors and regulatory bodies to uphold quality and compliance. Ideal candidates will bring substantial experience in clinical trial environments and a scientific background, fostering impactful collaborations in a dynamic setting.

Qualifications

• Experience as a Project Manager in international clinical trials within a CRO environment.
• Extensive experience managing global clinical trials in radiopharmaceuticals, gastrointestinal cancer, lung cancer, or breast cancer.
• Bid defense experience.

Responsabilités

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

Connaissances

Analytical skills

Organizational skills

Communication skills

Formation

Bachelor’s Degree in a science-related discipline

Description du poste

Company Description

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

Since its founding 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.
• Liaise with project team members, provide training as needed, and ensure correct task allocation.
• Develop, review, and update project plans to align with goals and milestones.
• Organize and facilitate project meetings related to study activities (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, other CROs, sponsors, and committee meetings (e.g., EC/IRB).
• Develop, review, and update SOPs to ensure regulatory compliance and develop study-related training programs.
• Contribute to bid defense activities.

Qualifications:

• Experience as a Project Manager in international clinical trials within a CRO environment.
• Extensive experience managing global clinical trials in radiopharmaceuticals, gastrointestinal cancer, lung cancer, or breast cancer.
• Bid defense experience.
• Strong analytical, organizational, and communication skills.
• Bachelor’s Degree in a science-related discipline.

Additional Information

Our core values guide our operations. If these resonate with you, Ergomed is a great place to join!

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

We look forward to receiving your application.