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7 days ago
JRF offers comprehensive nonclinical GLP research services for regulatory submissions, worldwide. JRF offers fast, transparent, cost-effective, and hassle-free services in Toxicology, Eco-toxicology, Chemistry, Environmental Fate and Metabolism, and other regulatory testing requirements.
**Responsibilities**:
- Participate and learn while conducting the scientific Regulatory Research/ studies, as per the Organizational requirements.
- Assist the Study Director and subsequently learn to operate the required instruments and machineries for performing the required research work.
- Assist the study Director in preparing and maintaining the required regulatory data.
- Ensure that studies are of the best quality and carried out in an expeditious manner.
- Constantly work towards improving self-competency; effectively maintain the performance improvement activities within the section.
**Qualification**:
- **Relevant Experience**: 0-2 years
- **Education**: M. Sc. (Zoology/Toxicology/Pharmacology/Life science), M.V.Sc.
- **Computer Skills**: Proficient.
- **Other skills**: Teamwork and Collaboration
- Knowledge of conducting of animal toxicology studies mainly repeated dose toxicity studies.
- Should be aware of animal handling and care
- Should be aware of dosing procedure by different routes in different in different species.
- Should be aware of different regulatory requirement for toxicology studies.
- Should have experience in working under GLP conditions.
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