Clinical Research Associate II

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

📋 Description

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

• Ensure that clinical studies are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and applicable regulations and standards.

• Coordinate the necessary activities to establish and monitor studies.

• Identify and select investigators for studies.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study assessments and initiation visits.

• Monitor sites within Belgium and provide occasional support to sites in the Netherlands.

• Recognize potential risks associated with studies and suggest mitigation strategies.

• Prepare for investigator meetings, site visits, and updates for the project team.

⛳️ Requirements

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

• A minimum of 2 years of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated skills.

• Experience in site management or a similar role within clinical research.

• Willingness to travel domestically, including overnight stays.

• Availability for approximately 50–60% travel commitment.

• Exceptional communication and organizational abilities.

• A collaborative team-player attitude.

• A client-focused mindset.

• Proficiency in both English and Dutch.

🏝️ Benefits

• Position allows for remote work.

• Reasonable travel requirements and enhanced work/life balance.

• Fewer protocols to manage than the industry average.

• Strong support from direct line management.

• Opportunity to make a significant impact and influence within a smaller CRO.