Study Director, Pharmacology & Toxicology

This role involves leading and managing preclinical study programs, ensuring scientific integrity and regulatory compliance. The Study Director will oversee all aspects of study conduct, from protocol development to final report generation, collaborating with cross-functional teams to deliver high-quality data and support drug development initiatives.

Key Responsibilities:

Lead and manage preclinical study programs, ensuring adherence to protocols and regulatory guidelines.
Develop and review study protocols, reports, and other scientific documents.
Oversee study monitoring and data review activities.
Collaborate with internal teams and external contract research organizations (CROs).
Ensure data integrity and compliance with Good Laboratory Practice (GLP) regulations.
Provide scientific expertise and guidance to study teams.

Requirements/Qualifications:

Advanced degree (Ph.D., M.S., or equivalent) in Pharmacology, Toxicology, or a related scientific discipline.
Significant experience (3-6 years) in preclinical study management.
Strong understanding of GLP regulations and study conduct principles.
Excellent communication, leadership, and problem-solving skills.
Ability to work effectively in a team environment.

About the Company: Sarthee Consultancy provides specialized services to the pharmaceutical and biotechnology industries. They focus on supporting clients with scientific and technical expertise throughout the drug development lifecycle.