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

📋 Description

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

• You will facilitate all essential activities required for the setup and monitoring of a study, which includes 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.

• A minimum of 2 years as a Clinical Research Associate (CRA) within a CRO or the pharmaceutical/biotech sector, or equivalent relevant experience and/or demonstrated competencies. Experience in site management or a related area in clinical research is also acceptable.

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

🏝️ Benefits

• A collaborative team player.

• Demonstrated client-focused approach.

• Willingness to travel domestically, including overnight stays, which may represent approximately 50-60% of travel commitment (some senior-level positions may involve international travel).

• Proficiency in English and Dutch.

• Knowledge of French is considered an advantage.

• Experience in oncology monitoring is a plus.