Job in Icon Clinical Research as Trip Report Reviewer
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Track record of successful management of the Clinical Operations aspects of regional/global studies/programs especially extensive experience reviewing trip report
US/LATAM/CAN: A minimum of five years of clinical research experience with at least four (4) years as a LCRA/CTM managing and reviewing trip report
EU/APAC: Proven, in-depth experience of clinical trial research experience with significant experience of clinical trial management
Should be a strong team player with a positive approach to managing people and project- or process related issues which are necessary to perform successfully in a service-oriented environment
Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials
Fluent in written and spoken English.
Ability and willingness to travel if required
Due to the nature of this position it may be required for the employee to travel. Therefore, dependent on the employees location, the employee may be required to possess a valid Drivers license
Extensive use of telephone expected
University/Bachelors Degree in medicine, science or local equivalent
Experience: Min. 4 years
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date: 31st July, 2014
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