Syngene Hiring Study Director for GLP In-Vivo Toxicology

Syngene Hiring Study Director for GLP In-Vivo Toxicology | MVSc / M.Pharm | 3-12 Years Exp | Bangalore

Take the lead in GLP-compliant toxicology research at Syngene! We are hiring a highly skilled Study Director to join our Safety Assessment team based in Bangalore. This pivotal role offers the opportunity to spearhead preclinical studies that shape the future of global healthcare.

Drive Scientific Excellence in Preclinical Safety

Syngene International, a leading biopharmaceutical research organization, invites applications from passionate professionals eager to contribute to rigorous in-vivo toxicology research. As a Study Director, you will manage toxicology studies from start to finish, ensuring adherence to global regulatory standards such as ICH and OECD guidelines.

Role: Study Director – GLP In-Vivo Toxicology

Location:

Syngene International, Bangalore

Experience:

3 to 12 Years

Qualification:

MVSc / M.Pharm (Pharmacology preferred)

Key Responsibilities

• Lead and oversee acute and repeated dose in-vivo studies.
• Serve as the single point of control for each study from planning to reporting.
• Ensure compliance with GLP principles and international regulatory standards.
• Interpret complex scientific data and communicate findings effectively.
• Review study protocols and collaborate with cross-functional teams.

Preferred Skills

• Strong background in pharmacology, toxicology, or preclinical research.
• Excellent understanding of ICH and OECD guidelines.
• Scientific documentation and regulatory compliance expertise.
• Effective communication and leadership abilities.

How to Apply

Send your updated resume to: minakhi.bhowmick@syngeneintl.com
Subject: Application for Study Director – GLP In-Vivo Toxicology

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