Description
Description:
This role is responsible for managing pharmacology studies and laboratory activities to support drug discovery, development, and regulatory submissions. The role oversees the design and execution of in vitro and in vivo pharmacology experiments, data analysis, and interpretation to evaluate safety, efficacy, and mechanism of action of pharmaceutical compounds. The incumbent ensures compliance with GLP, ethical standards, and regulatory requirements while maintaining data integrity and accurate documentation. It supports study planning, protocol development, and reporting, contributing to high-quality scientific outcomes. The role also drives continuous improvement in study execution and provides guidance and mentoring to junior team members to strengthen pharmacological and analytical capabilities.

Essential Functions:
Design, plan, and oversee in vitro and in vivo pharmacology studies to evaluate drug efficacy, safety, and mechanism of action
Review and interpret experimental data,



ensuring scientific accuracy and reliability of results
Ensure compliance with GLP, ethical guidelines, and regulatory requirements in all pharmacology activities
Prepare and review study protocols, reports, and regulatory documentation
Maintain accurate, complete, and timely documentation of experimental data and observations
Support cross-functional collaboration with R&D;, toxicology, and clinical teams for integrated drug development
Monitor laboratory operations, ensuring proper use of equipment, materials, and study procedures
Identify and implement process improvements to enhance study quality, efficiency, and data robustness
Mentor and guide junior staff to build technical and scientific competencies
Ensure adherence to safety standards, laboratory practices, and internal quality systems

Additional Responsibilities:

Qualifications
Education: M. Pharm (Pharmacology)
Experience: 8 years or more s

📌 Assistant Manager, Pharmacologist Ahmedabad (India)
🏢 Amneal
📍 India