Assistant Professor of Pharmacology

Description

Shifa Tameer-e-Millat University seeks a dedicated Assistant Professor of Pharmacology with at least two years of relevant experience to join its academic faculty. This role focuses on delivering high-quality education, engaging in impactful pharmacological research, and contributing to drug development initiatives. The position demands expertise in pharmacokinetics, pharmacodynamics, toxicology assessment, and clinical trial management. The successful candidate will be responsible for preparing and delivering lectures, supervising student research, and advancing scientific knowledge in pharmacology through rigorous data analysis and interpretation. The Assistant Professor will uphold the highest standards of regulatory compliance and documentation, ensuring all research activities adhere to established guidelines and quality management standards, including ISO 9001. Although this role does not involve managing a team, it requires collaborative interaction with other faculty members and research staff to foster an enriching academic environment and promote interdisciplinary projects. The candidate will also conduct in-vitro toxicology assays and contribute to preclinical testing phases essential for drug development processes.

Responsibilities

• Develop and deliver undergraduate and postgraduate lectures in pharmacology with clarity and engagement.
• Design and supervise laboratory sessions, ensuring hands-on learning in pharmacological techniques and assessments.
• Conduct independent and collaborative pharmacological research aimed at advancing drug development and safety evaluation.
• Perform data analysis and interpretation with scientific rigor to validate research findings and support publications.
• Manage preclinical testing protocols including pharmacokinetics, pharmacodynamics, and toxicology assessments.
• Conduct in-vitro toxicology assays to evaluate drug safety and efficacy in compliance with established procedures.
• Prepare and oversee documentation and reporting to maintain regulatory compliance throughout research projects.
• Ensure alignment of research activities with ISO 9001 quality management standards to maintain institutional quality benchmarks.
• Support clinical trial management activities by coordinating study design, data collection, and monitoring compliance.
• Collaborate with faculty and research teams to foster interdisciplinary approaches in pharmacological studies.
• Mentor and guide students in research methodology, experimental design, and scientific writing.
• Participate in curriculum development and continuous improvement of pharmacology courses and programs.
• Stay updated on advancements in pharmacology and related fields to integrate contemporary knowledge into teaching and research.

Experience

2 Years

Apply By

Oct 28, 2026

Required Skills

• Pharmacological Research
• Drug Development
• Preclinical Testing
• Toxicology Assessment
• Data Analysis and Interpretation
• Clinical Trial Management
• Pharmacokinetics and Pharmacodynamics
• Regulatory Compliance and Documentation
• In-vitro Toxicology Assays
• ISO 9001 Quality Management System