Toxicologist

Roles and Responsibilties:
1. As a Study Personnel, you should be knowledgeable in Principles of Good Laboratory Practice and ISO/IEC 17025:2017 and applicable study guideline/document which are applicable to your involvement in the study.

2. Adhere to the study plan and appropriate Standard Operating Procedures applicable to your involvement in the study, comply with the instructions given in those documents, document and report any deviation from these instructions directly to the Study Director, and/or if appropriate, the Principal Investigator(s).

3. You are responsible for recording raw data promptly, legibly and accurately and in compliance with these Principles of Good Laboratory Practice and ISO/IEC 17025:2017 and you will be responsible for the quality of their data.

4. As a study personnel, you should exercise health precautions to minimise risks and to ensure the integrity of the study. You should communicate to the appropriate person any relevant known health or medical condition in order that they can be excluded from operations that may affect the study.

5. Assisting the study director in preparation of study plan, any amendments and SOPs.

6. Providing study plan and any amendments to QAU.

7. Assure that study plans, amendments and SOPs are available and being used during the conduct of the study.

8. Preparation of study files with required formats for recording the raw data.

9. Preparation of study schedule with the help of study director.

10. Requesting for animals to animal facility in-charge.

11. Assure experimental room preparation before study initiation.

12. Assure provision of adequate quantity of feed and water to the animals.

13. Body marking of experimental animals, Measurement of body weight and feed consumption of experimental animals.

14. Dosing the animals, observation of clinical signs, to assist in anaesthetising the animals for blood collection.

15. Preparation for blood collection and necropsy and communicating the respective department.

16. Use and maintenance of instruments during the conduct of the study and completion of required log books / formats after use.

17. Archiving of study files and specimens (tissues, blocks and slides) Any other responsibilities entrusted by HOD/Study Director as required time to time.

18. To assist the study director in preparation of Part- B protocols.

19. Any other responsibilities entrusted by HOD as required time to time

20. Undergoing trainings and updating training files (External and Internal).

Qualification : Bachelor's or Master's in Pharmacology or Toxicology

Experience: Minimum 2 Years

Location: Barwala, Haryana

Job Type: Full-time

Pay: ₹12,000.00 - ₹25,000.00 per month

Benefits:

• Paid time off
• Provident Fund

Work Location: In person