Docs is hiring an experienced CRA to work on behalf of an international pharmaceutical company.
Roles & Responsibilities of the position
In the role of CRA you will be :
Responsible for planning, coordination and communication
Has major influence on the reputation and the results of the department, Region and company through motivational interaction with the site staff.
Always bear in mind that customer satisfaction is the ultimate departmental and individual goal. Efficiency, quality and job satisfaction should always be safeguarded to the same extent.
Actively contribute to adequate and timely information of all concerned within and outside the department.
Filing and archiving trial documentation in the Sponsor Trial Master File (STMF)
Monitor and communicate internally any site observations critical to business results
Maintain knowledge of and act in compliance with global and local SOPs, GCP and other regulatory requirements
Support audits and inspections at sites and affiliate, as applicable
Bachelor Degree in Life Sciences Minimum of 2 year experience as CRA in monitoring international clinical trialsLooking for a CRA interested in Endocrinology with / without experience in this therapeutic area.
Fluent English and local language
Remuneration & other details
We offer a long term collaboration, ideally 1 FTE, client office based or Home basedTo apply please send your CV to vera.stellino docsglobal.com
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