[Hiring] Clinical Research Associate II @Precision Medicine Group

Role Description

We are now recruiting a Clinical Research Associate II to join our team in Belgium or the Netherlands. This is a remote-based position with travel to sites for morning visits. We are looking for candidates based in Belgium or the Netherlands with oncology monitoring experience.

• You will monitor and own the progress of clinical studies at investigative sites.
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; help prepare regulatory submissions, conduct pre-study and initiation visits, etc.).

Qualifications

• Minimum Required:
• Life science degree and/or equivalent experience.
• 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
• Site management or equivalent experience in clinical research.
• Experience managing oncology studies.
• Other Required:
• Excellent communication and organizational skills are essential.
• A team player.
• Evidence of a client-focused approach.
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions).
• Fluency in English, Dutch; French will be a plus.
• Preferred:
• Study start-up activities experience.

Requirements

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared for investigator meetings, site visits, or project team updates.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility for the quality and outcomes of your work.
• You are adept at handling conflict using tried and true resolution strategies.

Benefits

• Lower than average number of protocols, setting you up to be a protocol expert.
• Reasonable travel and improved work/life balance.
• Your voice will be heard, allowing you to have influence and impact when it matters most.
• Support from direct line management.