Preclinical scientist

Role & responsibilities

1. Profound knowledge of preclinical regulatory guidelines.

2. Designing of preclinical studies as per the regulatory requirements to support the clinical bridging.

3. Preparation and review of preclinical study synopsis, study protocol and reports.

4. Preparation and Review of non-clinical overviews

5. Providing literature support for preclinical regulatory queries and regulatory literature search for various drug molecules.

6. Able to travel for monitoring the preclinical studies executed in different CROs.

Contacting the CROs for getting the quotations and time lines for the preclinical studies

Preferred candidate profile

Perks and benefits