Study Director -In-vivo Toxicology

Syngene

3 - 8 years

4 - 8 Lacs

Bengaluru

Posted:5 hours ago| Platform:

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Skills Required

Toxicology GLP Invivo Acute MVSc

Work Mode

Work from Office

Job Type

Full Time

Job Description

Core Purpose of the Role:

As a Study Director - Toxicology:

Responsible for ensuring that GLP toxicology studies; acute, repeat dose and reproduction are carried out to the required scientific and regulatory standards as per Global regulatory guidelines [ICH/OECD].
Function as single point of study control, overall responsibility for the scientific, technical and regulatory conduct of studies, scientific interpretation, documentation and reporting of results.

Role Accountabilities:

Study Director for in vivo toxicology studies
Coordination with local cross-functional teams like veterinary science, biopharmaceutics, bioanalysis, pharmacokinetics or in vitro biology before, during and after execution of toxicology studies
Conduct of in-life phases of toxicology studies in rats, mice and rabbits
Dose administration in rats, mice and rabbits with various routes of administration
Use of on-line data capture system- Pristima
Blood sample collection for toxicokinetic
Assistance during necropsy activities such as organ weighing, data entry in PROVANTIS software
Assistance in conducting rabbit electrophysiology studies
Coordination with veterinary science team IAEC meetings- preparation and maintenance of FORM-B and FORM-D
Blood collection in rats and mice via different routes for clinical pathology analyses
Preparation and following of in-house SOPs
Co-ordination for preventive maintenance and calibration of instruments.
Archival of materials from toxicology studies.
Any other duties given from time to time by the line manager

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