Research Director, Pharmacokinetics
Bengaluru, India (Also available in additional locations)
Full-Time | Office-Based
Job ID: R1481439
Lead and perform pharmacokinetic (PK) and pharmacodynamic (PD) analysis for Phase I-IV clinical pharmacology studies. Provide consultation on study design, clinical development strategy, and dossier submissions. Support strategic initiatives and mentor junior team members in Clinical Pharmacology.
Design and oversee analysis for studies including:
Dose tolerance and dose proportionality
Mass balance and bioavailability
Drug-drug interactions and QTc studies
Special populations (age, renal/hepatic impairment, gender)
Population PK/PD studies
Prepare clinical protocols, SAPs, analysis reports, and data visualizations (tables/listings/figures)
Author PK/PD sections for global regulatory dossiers
Deliver high-quality PK/PD outputs to clients within agreed timelines
Update Project Managers on deliverables’ progress
Serve as a key contact for clients, external vendors, and internal IQVIA departments
Work in multidisciplinary teams alongside PMs, CRAs, Data Managers, Statisticians, Programmers, and Medical Writers
Support proposal development and budget estimation for PK/PD study components
Provide mentorship, training, and guidance to junior pharmacokinetics staff
Contribute to implementation of quality control procedures
Drive strategic initiatives and process improvements
Stay current with scientific literature and industry trends
Attend relevant professional meetings and apply new technologies
Perform other duties as assigned by Clinical Pharmacology management
Education | Experience |
---|---|
PhD in Pharmacokinetics, Pharmaceutics, or related field | Minimum 5 years of relevant experience |
OR Master’s Degree / PharmD in Pharmacy or related field | Minimum 7 years of relevant experience |
OR Equivalent combination of education, training, and experience | – |
Technical Knowledge:
Noncompartmental and population PK/PD analysis
Familiarity with tools: WinNonlin, SigmaPlot, NONMEM, S-Plus, SAS
Drug Development Knowledge:
Deep understanding of ICH-GCP and international regulatory standards
Communication & Leadership:
Strong written/verbal communication
Mentoring and coaching abilities
Project Management:
Ability to prioritize and manage multiple PK/PD project components
Competence in working within a cross-functional matrix and multicultural environment
Interpersonal Skills:
Strong analytical thinking, organization, and collaboration capabilities
IQVIA is a global leader in clinical research, analytics, and technology solutions for the life sciences industry. IQVIA empowers healthcare innovation by combining deep data expertise with advanced technology and human insights to improve patient outcomes globally.
🌐 Learn more: https://jobs.iqvia.com
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