Senior Clinical Research Associate

This is a fully remote position, open to applicants in France, +4 more countries.

📋 Description

• Oversee and take ownership of the progress of clinical studies at investigative sites.

• Ensure that clinical studies are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

• Coordinate the setup and monitoring of studies, including identifying investigators, assisting in the preparation of regulatory submissions, and conducting pre-study and initiation visits.

• Manage clinical trials of appropriate scale.

• Provide support to larger clinical study teams.

• Train and guide junior team members.

• Engage directly with clients.

• Initiate payment processes.

• Contribute to proposal activities, including development and client presentations.

⛳️ Requirements

• Bachelor's degree or equivalent experience.

• Possession of a CRA certification.

• At least 5 years of CRA/SCRA experience in a CRO, pharmaceutical, biotechnology, or medical device setting.

• Proven experience in monitoring clinical trials across various therapeutic areas.

• Willingness to travel domestically, including overnight stays, approximately 50–60%; some senior-level positions may require international travel.

• Proficiency in English and the local language.

• Knowledge of additional languages is a plus.

• A graduate or postgraduate degree with a focus on a scientific or healthcare discipline is preferred.

• Experience with study start-up activities is preferred.

• Understanding of financial management is preferred for Senior CRAs.

🏝️ Benefits

• Opportunities for professional development.

• Potential for career advancement.

• Meaningful client relationships and a significant impact on clinical development.

• Fully remote work arrangement within France.

• Domestic travel, including overnight stays, as part of the role.