Clinical Research Associate II

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

📋 Description

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

• Coordinate all essential activities needed to initiate 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 2 years of experience as a CRA in a CRO or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies. Experience in site management or equivalent clinical research experience is preferred.

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

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

• Proven ability to maintain a client-focused approach.

• Willingness to travel domestically, which may involve approximately 50-60% of travel commitment (international travel may be required for certain senior-level positions).

• Proficiency in English and Dutch.

• French language skills would be an advantage.

• Experience in oncology monitoring would be a plus.

🏝️ Benefits

• Reasonable travel commitments and a favorable work/life balance.

• Your input will be valued.

• Working within a smaller CRO provides opportunities for influence and impact when it matters most, along with support from direct line management.