Clinical Research Associate

September 16

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QPS Holdings, LLC

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Custom-built Research Services: supporting drug discovery, preclinical, bioanalysis and clinical trial needs.

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

1001 - 5000

💰 Private Equity Round on 2010-12

Description

• Monitor clinical drug studies according to guidelines • Manage studies from initiation to close-out • Communicate with clients and conduct site visits • Verify data and check drug accountability • Review execution and processes at study sites

Requirements

• Bachelor's degree or equivalent academic level • Experience in the CRO field is a plus • Prior CRA work experience, specifically monitoring clinical trials • Strong communication skills in Dutch and English • Willingness to travel to clinical trial sites • Proactive with attention to detail

Benefits

• Full-time position of 32-40 hours per week • Opportunity to work from home in Netherlands or Austria • Potential for extension after one year • Participation in QPS vaccination program