Covance

Clinical Research Assosiate

CH
Job Number
2017-14778
Job Category
Clinical Research Associate
Position Type
Full-Time

Job Overview

We are currently recruiting for a Clinical Research Associate II in Switzerland for our Clinical Operations team.
As an experienced CRA you’ll be involved in initiation, routine & close out visits concentrating on sites in Switzerland. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE.

Requirements:
- Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Excellent understanding of Serious Adverse Event reporting
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in Switzerland
- Fluency in speaking and writing German/French/Italian and English
- Oncology experience is a nice to have

Education / Qualifications

Degree in life sciences OR equivalent experience in clinical monitoring

Experience

Minimum Required:
• In lieu of the above requirements, candidates with supervisory experience in a health care setting and clinical research experience in the pharmaceutical or CRO industries (including monitoring) may be considered
• Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Advanced site monitoring skills
• Advanced study site management skills
• Advanced registry administration skills
• Ability to work with minimal supervision
• Good planning and organization skills
• Good computer skills with good working knowledge of a range of computer packages
• Advanced verbal and written communication skills
• Ability to train and supervise junior staff
• Ability to resolve project-related problems and prioritizes workload for self and team
• Ability to work within a project team

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