Freelance Clinical Research Associate (France)

Join us in redefining what it means to work for a CRO.  

When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. 

Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. 

You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.

We are currently hiring a Freelance Clinical Research Associate in France for circa. 0.1 FTE to join our amazing team! In this role, you will have the opportunity to manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files. You’ll also ensure the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget.

 Our Clinical Operations Team will tell you that joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

What You'll Be Doing:

• Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines
• Conduct of country and site feasibility
• Site initiation, routine monitoring and close-out visits
• Preparation and submissions to Ethics Committees/Regulatory Authorities
• Assistance in site contract management

Requirements

• University degree in medicine, pharmacy, nursing or life science and at least 2 years of previous on-site monitoring experience in CRO or Pharma company; previous freelancing experience will be considered as an advantage; previous experience in preparation and submissions to Ethics Committees / Regulatory Authorities.
• Strong Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho’s. Fluency in both English and local languages.
• Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.
• High-Character: Contribute to our collaborative culture with honesty and integrity. At Rho, we value a strong team spirit highlighted by loyalty, accountability, and mutual trust. We work smart together, we work hard together, and we laugh together. We take responsibility for our actions, forgive honest mistakes and respect one another.
• Critical Thinker: Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. We evaluate situations and opportunities objectively and incisively; we then craft novel, practical solutions.
• Agile and Adaptable: Rho values the ability to change quickly. We eagerly anticipate, respond to, and take advantage of changes in our environment. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. The opportunity to adapt and evolve energizes us.
• Driver license and ability to travel

 Please submit your CV in English. We’re excited to hear from you!

 We offer:

• A job with daily exciting challenges in a highly qualified and international team
• Employee-friendly work environment
• Competitive salary
• Opportunity to learn and grow professionally in Clinical Research field