Clinical Research Associate - CRA

November 7

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Logo of QPS Holdings, LLC

QPS Holdings, LLC

DMPK • Translational Medicine • Toxicology • Bioanalysis • Phase II - IV Clinical Development

1001 - 5000

💰 Private Equity Round on 2010-12

Description

• Monitor clinical drug studies across various research centers. • Manage studies from site initiation to close-out, conduct regular site visits and write reports. • Verify data, check study drug accountability, and discuss study progress with site staff. • Work independently and as part of a team during visits to research centers.

Requirements

• Extensive, hands-on experience managing all facets of clinical trial monitoring. • Ideally hold a bachelor’s degree or equivalent academic level. • Proficiency in both Dutch and English, spoken and written required. • Must be able to travel to assigned clinical trial sites, occasionally involving overnight stays. • Detail-oriented professional who works with precision and organization and communicates effectively. • Proactivity and an eye for detail are essential.

Benefits

• Full-time position of 32-40 hours per week for at least one year. • Opportunity for extension after one year. • Work from home office in the Netherlands or Austria!

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