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Research Associate I (Study Director) Toxicology Department

1-5 years
Not Disclosed
10 Nov. 7, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Associate (Study Director) - Toxicology

Location: Jubilant Biosys
Department: Toxicology


About Jubilant Biosys

Jubilant Biosys is a part of the Jubilant Pharmova family, providing comprehensive drug discovery and contract research services. With a focus on oncology, metabolic disorders, CNS diseases, and pain & inflammation, Jubilant Biosys has established itself as a leading collaborator for pharmaceutical and biotech companies worldwide. The company offers deep expertise in medicinal chemistry, discovery informatics, structural biology, and translational sciences.

For more information, visit www.jubilantbiosys.com.


Position Overview

Designation: Research Associate (Study Director)
Department: Toxicology
Experience: 1-5 Years
Qualification: Masters in Veterinary Science (MVSc), M.Pharm, MSc

The Study Director is the primary point of control for studies conducted in the Toxicology department. This role ensures Good Laboratory Practice (GLP) compliance and oversees the conduct of genetic toxicology studies. As the Study Director, you will be responsible for ensuring that studies are completed within expected timelines and meet all required regulatory standards.


Key Responsibilities

  • Study Direction: Oversee and direct the conduct of in-vitro genotoxicity and phototoxicity studies.
  • Compliance: Ensure strict adherence to Good Laboratory Practice (GLP) regulations.
  • Team Communication: Maintain effective communication with team members and Toxicology Functional Management (TFM) to ensure smooth project execution.
  • Study Execution: Conduct and lead various genetic toxicology studies, including Ames, Mini Ames, MNT, Chromosomal Aberration Tests, and Phototoxicity Studies.
  • Laboratory Experience: Contribute to day-to-day operations in the GLP laboratory, leveraging at least 2 years of GLP experience.
  • Timeline Management: Ensure studies are completed on time and meet all quality expectations.

Qualifications & Experience

  • Education: Masters in Veterinary Science (MVSc), M.Pharm, or MSc in a related field.
  • Experience: Minimum of 1-5 years in a GLP laboratory with hands-on experience in conducting genotoxicity and phototoxicity studies.
  • Technical Skills: Proficient in performing Ames, Mini Ames, MNT, chromosomal aberration, and phototoxicity tests.

Why Join Us?

  • Cutting-edge Research: Be part of a growing team that conducts impactful studies in genotoxicology and toxicology.
  • Career Growth: Advance your career in a dynamic, fast-paced environment.
  • Global Impact: Work in an organization that collaborates with leading pharma and biotech companies worldwide.

Equal Opportunity Employer

Jubilant Biosys is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, ethnicity, gender, disability, or any other characteristic protected by law.