Clinical Research Associate (CRA)

About this job

The main task of the CRA is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house at bioskin or in the Northern German region. Your main responsibilities: Perform all kind of the monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoring Generation and updating of monitoring plans and site initiation presentation Evaluating the quality and integrity of site practices Act as contact for clinical trial suppliers and other vendors as assigned Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols Close cooperation with the different departments in-house at bioskin as well as…

This is a short summary.

Want to know if you're a fit? Check your CV against this role — free, in 30 seconds.

Salaries in Hamburg

Based on 122 postings that disclose pay.

Estimated from advertised pay across our sources — indicative gross annual figures, not an offer.

Similar jobs

• Backend Developer - Golang (f/m/d) · Justdice
• Werkstudent (m/w/d) Information Security · dpa Deutsche Presse-Agentur GmbH
• Senior Technical Service Manager (m/w/d) · dpa Deutsche Presse-Agentur GmbH
• EU Freelancer (m/w/d) - Inbound Customer Service - 100% Homeoffice - EU, außerhalb DE · hey contact heroes GmbH
• DC Team Leader (m/w/d) Lagerlogistik in der Spätschicht – Vollzeit, unbefristet · H&M
• (Senior) Project Manager AY Commerce (all genders) · ABOUT YOU SE & Co. KG