Remote CRA II – Oncology & Rare Disease

Pfm; United States; Remote; USD 56,000 - 78,000; Full time

Benefits offered by this job

Remote work option

Job summary

Precision Medicine Group in the Netherlands seeks a Clinical Research Associate II to monitor studies at investigative sites, ensuring compliance with protocol, SOPs, ICH-GCP and applicable regulations.

This remote-based role requires biopharma monitoring experience, flexibility for travel, and fluency in English and Dutch; French is a plus. You will work with a passionate team in a smaller CRO that values input and impact.

Qualifications

• Life science degree required.
• 2+ years as a CRA in CRO or pharma/biotech industry.
• Willingness to travel domestically and internationally (up to 50-60% travel).

Responsibilities

• Monitor progress of clinical studies at investigative sites per protocol and ICH-GCP.
• Coordinate all activities to set up and monitor a study (identify investigators; regulatory submissions; pre-study visits; initiation visits).
• Identify study risks and propose mitigation strategies to ensure quality and outcomes.

Skills

Communication skills

Organizational skills

Client-focused approach

Fluency in English and Dutch

Willingness to travel

Education

Life science degree

2+ years CRA experience

Job description

Precision Medicine Group in the Netherlands seeks a Clinical Research Associate II to monitor studies at investigative sites, ensuring compliance with protocol, SOPs, ICH-GCP and applicable regulations.

This remote-based role requires biopharma monitoring experience, flexibility for travel, and fluency in English and Dutch; French is a plus. You will work with a passionate team in a smaller CRO that values input and impact.