Clinical Research Associate I/II

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

📋 Description

• Oversee and take responsibility for the advancement of clinical studies at investigative sites.

• Ensure that clinical studies are carried out, documented, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP guidelines, and all relevant regulations and standards.

• Coordinate all essential activities needed to establish and monitor a study, including identifying investigators, assisting in the preparation of regulatory submissions, and conducting pre-study and initiation visits.

⛳️ Requirements

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

• At least 1 year of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or within the pharmaceutical/biotech industry, or equivalent relevant experience and/or proven competencies. Experience in site management or similar roles in clinical research is also acceptable.

• Experience in managing oncology studies.

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

• Strong communication and organizational skills are crucial. Must be a team player.

• Demonstrated client-focused approach.

• Proficiency in English, and for non-English speaking countries, fluency in the local language of the country where the position is based.

🏝️ Benefits

• Travel requirements are reasonable, contributing positively to your work/life balance.

• Support from direct line management.

• High retention rates for CRAs compared to industry averages.