Clinical Research Associate I/ II

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

📋 Description

• Oversee and manage the progress of clinical trials at investigative sites, ensuring that all studies are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

• Organize all essential activities necessary for setting up and monitoring a study, which includes identifying investigators, assisting with 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) within a CRO or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies, including site management or similar roles in clinical research.

• Proven experience in managing oncology studies.

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

🏝️ Benefits

• Strong communication and organizational skills are crucial, along with being a collaborative team member.

• Demonstrated commitment to a client-focused approach.

• Willingness to engage in domestic travel, including overnight stays, potentially amounting to approximately 50-60% travel commitment (some senior-level positions may necessitate international travel).

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