Job Description:
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.
Job 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
Only for Experience candidate:
- 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.
Salary: Negotiable for competent candidature.
