Project Manager II

We are looking for a Project Manager II F/M to join our Project Management team on a fixed-term contract to cover a maternity leave.

In this role, you will act as the primary operational lead for oncology clinical trials (Phase I to III) involving imaging endpoints. You will be responsible for driving the successful execution of projects from study start-up through close-out, ensuring the delivery of high-quality, compliant study data while meeting project timelines, budgets, and sponsor expectations.

Working in a highly collaborative and international environment, you will coordinate cross-functional teams across Imaging Operations, Data Management, Medical, Technical, and Site Management functions to ensure project success.

Key Responsibilities

• Lead and manage oncology clinical trial projects throughout their entire lifecycle.

• Serve as the main point of contact for sponsors and internal stakeholders.

• Develop and maintain project plans, timelines, budgets, risk management, and communication plans.

• Coordinate all imaging-related operational activities, including:

  • Study specification development

  • Imaging database implementation

  • Systems integration

  • Image collection and quality control

  • Independent reader management

  • Central review operations

  • Data management and sponsor deliverables

• Monitor project performance and proactively identify risks and mitigation plans.

• Ensure compliance with internal procedures, GCP guidelines, and project management best practices.

• Report project status, milestones, and risks to management.

• Support and mentor junior project team members when required.

• Contribute to business support activities, including budget estimations and proposal preparation.

Education

• Master's degree in Life Sciences, Biomedical Engineering, Clinical Research, or a related scientific field.

Experience

• Minimum 3 years of experience in project management.

• Experience within the pharmaceutical, biotechnology, CRO, medical device, or clinical research environment.

• Experience in clinical trials and/or medical imaging is highly desirable.

• Knowledge of oncology studies is a strong asset.

Skills

• Strong project management and organizational skills.

• Ability to manage multiple priorities and stakeholders in a dynamic environment.

• Excellent communication and interpersonal skills.

• Knowledge of clinical research processes and Good Clinical Practice (GCP).

• Understanding of medical imaging, data management, software development, or related healthcare technologies is a plus.

• Fluent English, both written and spoken. French is an advantage.

Median Technologies is committed to cultural diversity, gender equality and the employment of disabled workers.