Freelance Clinical Research Associate — Drive Study Excellence

Rho, Inc.; France; Hybride; EUR 20 000 - 40 000; Plein temps

Avantages offerts par ce poste

Competitive salary

International team

Résumé du poste

Rho, Inc. is hiring a Freelance Clinical Research Associate in France for circa 0.1 FTE to manage site selection, initiation, monitoring, and close-out, ensuring data quality and regulatory compliance.

You will work with an international team, travel as required, and contribute to studies across our clinical operations. This role offers flexibility, competitive compensation, and opportunities for career growth within our stable CRO environment.

Qualifications

• University degree in medicine, pharmacy, nursing or life science with at least 2 years on-site monitoring experience.
• Fluency in English and local languages.
• Freelance experience is an advantage; familiarity with Ethics Committees/Regulatory Authorities.

Responsabilités

• Site administration and monitoring for assigned studies per SOPs and ICH-GCP.
• Conduct country and site feasibility.
• Site initiation, routine monitoring and close-out visits.
• Prepare and submit to Ethics Committees/Regulatory Authorities.
• Assist in site contract management.

Connaissances

Strong Communicator

Committed to Quality

High-Character

Critical Thinker

Agile and Adaptable

Driver's license

Willing to travel

Fluent English

Formation

University degree in medicine/pharmacy/nursing/life science

Description du poste

Rho, Inc. is hiring a Freelance Clinical Research Associate in France for circa 0.1 FTE to manage site selection, initiation, monitoring, and close-out, ensuring data quality and regulatory compliance.

You will work with an international team, travel as required, and contribute to studies across our clinical operations. This role offers flexibility, competitive compensation, and opportunities for career growth within our stable CRO environment.