Assistant Manager, Pharmacologist (R&D Injectable)

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad seeks a senior pharmacology scientist to design, plan and oversee in vitro and in vivo studies evaluating drug efficacy, safety and mechanism of action.

You will review data, ensure GLP compliance and regulatory readiness, prepare protocols and reports, and mentor junior staff while driving data quality and process improvements across R&D teams.

Qualifications

• M. Pharm (Pharmacology) required.
• 8+ years of experience in pharmacology research.

Responsibilities

• 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

Skills

Pharmacology

Education

M. Pharm (Pharmacology)

Job description

Responsibilities

• 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

Qualification & Experience

• M. Pharm (Pharmacology)
• Experience: 8 years or more