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- You will be responsible for assisting in acute, repeat dose and reproduction toxicology studies and documentation of study data.
- You will be familiar with conducting all work in compliance with applicable regulatory requirements governing the work in which they are involved, such as GLP.
- Assist in conduct of study in compliance with the Principles of Good Laboratory Practice.
- Comply with the instructions given in the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study. Any deviation from these instructions should be documented and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s).
- Record raw data promptly and accurately and in compliance with Principles of Good Laboratory Practice, and ensure the quality of their data.
- Exercise health precautions to minimize risk to them and to ensure the integrity of the study. 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.
- You should have good understanding and hands on Experience of toxicology. Preferably have knowledge of related disciplines, toxicokinetics, pathology and analytical chemistry.
- Ideally, you should be working in or have experience within contract research, pharmaceutical companies or have an academic background related to a toxicology discipline.
- A proactive attitude towards internal and external customer satisfaction and the highest standards of scientific quality and regulatory compliance.
- Good written and spoken communication skill.
- Have a meticulous attitude towards consistency of 100% quality in study plan, reports and related material.
- Be aware of study status at all times and anticipate problems that may affect timing, quality or integrity and take appropriate action to resolve such problems.
- Basic familiarity with Microsoft Office Suite.
- Computer skills, commensurate with Essential Functions and including ability to learn a validated system.
- Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
- Ability to work under specific time constraints.
Associate Scientist - Bengaluru, India - Syngene
Description
JOB PURPOSE (Briefly describe the objectives of the job):
As a Study Personnel - Toxicology:
KEY RESPONSIBILITIES :
EDUCATIONAL QUALIFICATION:
To be successful in this position, you will need to hold a degree or above in a life sciences discipline (B.Sc./ M.Sc./ B.V.Sc./ M.V. Sc / M. Pharm).
WORK EXPERIENCE:
0 to 2 years of experience as study personnel.
TECHNICAL /FUNCTIONAL SKILL:
BEHAVIORAL/MANAGERIAL SKILLS:
You need to demonstrate:
OTHER JOB REQUIREMENTS: