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Clinical Research Associate (CRA)

extra holidays - extra parental leave

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Netherlands

Offer summary

Qualifications:

Several years of clinical trials monitoring experience, Knowledge of GCP and WMO guidelines.

Key responsabilities:

Monitor clinical drug studies
Manage studies from initiation to close-out
Conduct regular site visits
Communicate with clients
Write reports and verify data

QPS Holdings, LLC Pharmaceuticals Large https://www.qps.com/

1001 - 5000 Employees

See more QPS Holdings, LLC offers

Job description

QPS Netherlands B.V. in Groningen is part of QPS Holdings, LLC - we conduct drug development activities on behalf of international pharmaceutical and biotechnological companies. QPS is building our Clinical Research department in Groningen and looking for candidates with several years of prior clinical trials monitoring experience for the position of Clinical Research Associate.

What will you do?

In this role, you will travel to and monitor clinical drug studies across various research centers according to applicable guidelines such as GCP and WMO. You will manage studies from site initiation to close-out, communicate with clients, conduct regular site visits, and write reports. You will verify data, check study drug accountability, discuss study progress and issues with site staff, and review various aspects of execution, processes, samples, and materials. You will work as part of a team but also independently during visits to research centers. When not traveling to a clinical trial site, you will work from home.