Clinical Pharmacology

About the Role

The Clinical Pharmacology professional will play a key role in designing, executing, and interpreting clinical and translational pharmacology studies within Livanity’s integrated research framework. This is a full-time, on-site role based in the Pune Division.

Key Responsibilities

• Developing clinical pharmacology plans for BA/BE and clinical trials.
• Evaluating PK-PD, DMPK, and drug interaction data.
• Contributing to protocol design, study documentation, and regulatory submissions.
• Collaborating with medical, regulatory, and scientific writing teams to ensure data integrity, ICH-GCP compliance, and alignment with personalized and integrative medicine approaches.
• Participating in cross-functional project meetings.
• Supporting training for study teams on clinical pharmacology concepts.
• Contributing to continuous process improvement.

Requirements & Tech Stack

• Strong foundation in Medicine and Clinical Pharmacology.
• Applied experience in Clinical Research across BA/BE and early- to late-phase studies.
• Demonstrated Research skills, including study design, data analysis, interpretation of PK-PD and safety data, and preparation of scientific and regulatory documents.
• Effective Communication skills, with the ability to present complex pharmacology concepts clearly to multidisciplinary teams and stakeholders.
• Experience in Training clinical and research staff on protocols, ICH-GCP, pharmacology principles, and data handling procedures.
• Familiarity with regulatory requirements for clinical pharmacology studies, including ICH-GCP and regional guidelines for EU, US, and Indian submissions.
• Proficiency in relevant analytical and statistical tools used for PK-PD and clinical data evaluation.
• Ability to work collaboratively in an integrative, multidisciplinary environment.

Qualifications

• Advanced degree in Pharmacy, Pharmacology, Medicine, or a related life science (e.g., M.Pharm, PharmD, MD, PhD) preferred.