Study Director (Toxicology)

Sipra Labs

5 - 10 years

4 - 9 Lacs

hyderabad

Posted:3 hours ago| Platform:

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Skills Required

toxicology glp pharmacology invitro study director in vitro

Work Mode

Work from Office

Job Type

Full Time

Job Description

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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