Clinical Research Associate I – Clinical Research Associate II

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

📋 Description

• Oversee and take responsibility for the advancement of clinical trials at investigative sites, ensuring that these studies are conducted, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• Organize all essential tasks needed to initiate and monitor a study (e.g., identifying investigators; assisting with regulatory submissions, executing pre-study and initiation visits, etc.)

⛳️ Requirements

• A degree in life sciences and/or equivalent experience.

• At least one year of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or within the pharmaceutical/biotech sector, or comparable relevant experience and/or demonstrated skills. Experience in site management or similar roles in clinical research.

• Proven experience in managing oncology studies.

• Willingness to travel domestically, including overnight stays as required (some senior-level positions may necessitate international travel).

• Strong communication and organizational abilities are crucial. A collaborative team player.

• Demonstrated client-focused mindset.

• Availability for domestic travel, including overnight stays, potentially constituting about 50-60% of travel commitment (some senior roles may require international travel).

• Proficiency in English; for positions in non-English speaking countries, fluency in the local language is required.

• Experience with study start-up activities.

🏝️ Benefits

• No explicit benefits listed.