Beschreibung
Clinical Associate (m/f/d)
Reference: -en
Start: asap
Duration: 6 MM+
Main tasks:
- Participate in the design, administration and monitoring of clinical trials
- Analyze and evaluates clinical data gathered during research
- Ensure compliance with protocol and overall clinical objectives
Main qualifications
- Knowledge of FDA regulatory requirements is required
- Bachelor's degree and several years of related experience
- May require ACRP or SOCRA Clinical Research Professional exam completion
Main advantages:
- Reputable international company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Yves Fabien Deschamps
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