Clinical Scientist (m/f/d)
Responsibilities
- Coordinating and overseeing an ongoing clinical trial
- Interpreting and implementing clinical trial protocols
- Ensuring compliance with regulatory requirements, analyzing data, and collaborating with cross-functional teams
Profile
- Solid experience in clinical development within biotech or pharmaceutical environments
- Strong experience in clinical data cleaning, particularly within ongoing trials
- Experience supporting Phase II clinical trials, including preparation of data for analysis after unblinding
- Ability to support data cleaning across multiple trials, including an ongoing rare liver disease study
- Experience in clinical trial coordination and CRO oversight
- PhD required
- Experience in rare disease or liver disease considered advantageous
Benefits
- Challenging and varied tasks in a promising and innovative industry
- Flat hierarchies
- Individual development opportunities
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in 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 experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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