Remote CRA II – Oncology Trials, Flexible Travel

Pfm; Netherlands; On-site; EUR 50,000 - 70,000; Full time

Job summary

Precision Medicine Group is recruiting a Clinical Research Associate II in the Netherlands. This remote-based role involves travel to sites for morning visits and requires a Life science degree with 2+ years of CRA experience in CRO/pharma settings.

Domestic travel up to 50–60% may be needed, with international travel possible for some senior positions. You will monitor studies, ensure compliance with protocols, SOPs, ICH-GCP, and regulatory standards, and coordinate site activation activities.

Qualifications

• 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.
• Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions).
• 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
• Oncology monitoring experience will be a plus

Responsibilities

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

Skills

Communication skills

Organizational skills

Team player

Client focused

Education

Life science degree

Job description

Precision Medicine Group is recruiting a Clinical Research Associate II in the Netherlands. This remote-based role involves travel to sites for morning visits and requires a Life science degree with 2+ years of CRA experience in CRO/pharma settings.

Domestic travel up to 50–60% may be needed, with international travel possible for some senior positions. You will monitor studies, ensure compliance with protocols, SOPs, ICH-GCP, and regulatory standards, and coordinate site activation activities.