Job in Icon Clinical Research as Trip Report Reviewer

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Role Requirements

  • 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.
  • Computer literate
  • 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

Additional Information:
Experience:
Min. 4 years
Location: Chennai
Reference: 010777

Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date:
31st July, 2014

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