Freelance CRA - France

  • Competitive
  • France, France
  • Contract
Eager to join the quest to conquer cancer? An exciting opportunity has arisen at a niche clinical research organisation (CRO). A CRO that are dedicated to going the distance to bring new therapies and vaccines to patients in need. Looking to make a real impact in a community based, family friendly CRO?
This CRO specializes in conducting early and late-phase oncology trials in the U.S, Europe and Asia. The ongoing association with NCI continues to be a strong basis for operations. The focus is cancer

Job Description
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to initiation, the development of a robust patient recruitment strategy, setting up a system, assessing compliance with regulations and the site’s capability to comply with the study needs and recruitment expectations, and problem solving to address and resolve site issues.

  • Develop and write trial protocols (outlining purpose and methodology)
  • Present trial protocols to a steering committee
  • Design data collection forms, known as case report forms (CRFs)
  • Coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects
  • Manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs
  • Identify and assess the suitability of facilities to use as the clinical trial site
  • Identify/select an investigator who will be responsible for conducting the trial at the trial site
  • Liaise with doctors, consultants or investigators on conducting the trial
  • Set up the trial sites - ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)

Skills required: 
  • A degree in life sciences
  • 2yrs independent monitoring experience upwards
  • Oncology experience
  • French speaking

Location: France

Rate: Flexible based on experience

FTE: 0.5 FTE upwards

This Role is an urgent need. So, the processes for these roles are moving very quickly so if there is an interest, we will need to move fast to ensure you don’t miss out.

These positions will be snapped up, looking for individuals who are ambitious, positive and want to work in a growing and exciting team.

Do not miss out on this opening – apply below or contact Kush at Meet on 0203 0195957 or email directly to
You can find out more about Kush & Meet at
Kush Obhrai Talent Partner

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