Study Director

2 weeks ago


Hyderabad, India Sipra Labs Full time
  • Preparation of study plan considering the client requirements as well as regulatory requirements.
  • Preparing a study schedule and communicating with all the study personnel and ensuring the proper conduct of the study.
  • Preparing reports after completion of each study. This involves evaluating the data output by applying scientific knowledge and skills.
  • To maintain the highest regulatory standards (OECD GLP) during any activity conducted in the facility by continuous monitoring and checkup of all the instruments/equipment used in a study as per Standard Operating Procedures (SOPs).
  • Preparation and periodic revision of Standard Operating Procedures.
  • Preparation and presentation of experiment conduct protocols to the Institutional Animal Ethics committee.
  • Periodically verify data generated during study.
  • Archival of the study plan, study report, raw data and related materials as per the study plan.
  • Coordinate with TFM and/or study personnel and keeping informed of their findings during the study and receipt and evaluation of their respective individual reports for inclusion in the final study report.

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