Syngene International, a premier biopharmaceutical research organization, is seeking a Study Director (GLP In-Vivo Toxicology) to join its Safety Assessment team in Bangalore. This role is critical for designing, executing, and overseeing preclinical toxicology studies in compliance with global regulatory standards (ICH, OECD, GLP).
Key Responsibilities:
- Lead acute and repeated dose in-vivo toxicology studies from protocol development to final reporting.
- Ensure adherence to Good Laboratory Practices (GLP) and regulatory guidelines.
- Serve as the primary point of contact for study execution, data interpretation, and stakeholder communication.
- Collaborate with multidisciplinary teams to deliver high-quality preclinical research.
- Maintain accurate scientific documentation for regulatory submissions.
About Syngene International
Syngene is a subsidiary of Biocon and a leading contract research organization (CRO) specializing in drug discovery and development. With state-of-the-art facilities in Bangalore, Syngene partners with global pharmaceutical companies to advance innovative therapeutics.
Eligibility Criteria
Education & Experience:
- MVSc (Veterinary Pharmacology/Toxicology) or M.Pharm (Pharmacology).
- 3–12 years of hands-on experience in GLP-compliant in-vivo toxicology studies.
- Strong knowledge of ICH, OECD, and FDA guidelines.
Preferred Skills:
- Expertise in preclinical study design, data analysis, and reporting.
- Excellent scientific writing and presentation skills.
- Leadership capabilities to manage cross-functional teams.
How to Apply
Interested candidates can apply by sending their updated resume to:
Email: minakhi.bhowmick@syngeneintl.com
Subject Line: “Application for Study Director – GLP In-Vivo Toxicology”
