Medreich Walkins

September 11th, 2015

Job Description
Planning and Execution Pilot and Pivotal bioequivalence studies
Responsible for coordinating and monitoring of all aspects of Bioequivalence studies.
Interacts, with Clinical Investigators, Contract Research Organizations (CROs), Contract Research Laboratories (CRL) to ensure that the quality of data meets the high standards specified in the Good Clinical Practices (GCP) guidelines and corporate Standard Operating Procedures (SOPs).

Role Clinical Research Associate/Scientist
Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Contact Medreich Limited

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