Freelance Clinical Research Associate

This is a fully remote position, open to applicants in France.

📋 Description

• Oversee all facets of study site management, which includes site selection, initiation, routine monitoring, close-out, and maintaining study files.

• Guarantee data quality and integrity, adherence to relevant SOPs and regulatory standards, and timely completion of studies within budget constraints.

• Execute site administration and monitoring for assigned clinical trials in accordance with Dokumeds and Sponsor SOPs, legal mandates, and ICH-GCP Guidelines.

• Conduct feasibility assessments for countries and sites.

• Perform site initiation, regular monitoring, and close-out site visits.

• Prepare and submit documentation to Ethics Committees and Regulatory Authorities.

• Support site contract management activities.

⛳️ Requirements

• Bachelor's degree in medicine, pharmacy, nursing, or a life science discipline.

• Minimum of 2 years of prior on-site monitoring experience in a CRO or pharmaceutical company.

• Freelance experience in the field will be regarded as a plus.

• Prior experience in the preparation and submission of documents to Ethics Committees and Regulatory Authorities.

• Excellent written, verbal, and presentation skills.

• Proficiency in both English and local languages.

• Meticulous attention to detail and a solid understanding of high-quality scientific standards.

• Traits of honesty, integrity, loyalty, accountability, mutual trust, and a strong team-oriented mindset.

• Strong critical thinking abilities and the capacity to develop innovative, practical solutions.

• Flexibility to adapt quickly, anticipate and respond to changes, and manage risks effectively.

• Valid driver’s license and willingness to travel.

• CV must be submitted in English.

🏝️ Benefits

• A role offering daily exciting challenges within a highly skilled and international team.

• A supportive and employee-friendly work environment.

• Competitive salary package.

• Opportunities for professional learning and growth in the Clinical Research field.