Research Director – Pharmacokinetics
Location: Bengaluru, India
Work Mode: Full-Time, Office-Based
Requisition ID: R1481439
Job Overview:
IQVIA is seeking a Research Director in Pharmacokinetics to lead and support the design, analysis, and reporting of pharmacokinetic (PK) and pharmacodynamic (PD) studies across all clinical phases (I–IV). The role involves providing scientific leadership, client consultation, regulatory support, and mentoring of junior staff, while ensuring high-quality project execution across a variety of therapeutic domains.
Key Responsibilities:
Lead or supervise development of protocols, SAPs, PK/PD analyses, and clinical study reports for:
Dose tolerance & proportionality
Bioavailability & bioequivalence
Mass balance & concept testing
QTc studies & drug-drug interactions
Special population studies (e.g., renal/hepatic impairment, gender/age effects)
Population PK/PD modeling
Collaborate with clients and internal teams to advise on clinical development plans, study designs, and regulatory submissions.
Contribute to global regulatory dossiers and communicate directly with regulatory bodies regarding PK/PD content.
Ensure timely, high-quality delivery of PK/PD-related outputs.
Provide regular project updates to internal project managers.
Serve as the PK/PD subject matter expert on cross-functional project teams.
Guide and mentor junior scientists, providing training and scientific oversight.
Support business development activities, including proposal and budget preparation.
Recommend, develop, and implement quality control procedures and scientific review strategies.
Stay updated with new developments, technologies, and regulations in Clinical Pharmacology.
Required Qualifications:
Ph.D. in Pharmacokinetics, Pharmaceutics, or related field (preferred), OR
Master's/PharmD in Pharmacy or related discipline
Minimum 5–7 years of experience in Clinical Pharmacokinetics or Clinical Pharmacology
Strong expertise in noncompartmental analysis and population PK modeling (e.g., using WinNonlin, NONMEM)
Familiarity with PK/PD software tools: WinNonlin, SigmaPlot, NONMEM, SPlus, SAS
In-depth understanding of GCP, ICH, regulatory guidelines, and clinical drug development
Ability to coordinate complex projects and meet timelines across global teams
Excellent communication, client-facing, and leadership skills
Proven problem-solving, analytical, and mentoring capabilities
Estimated Salary: ₹46,00,000 – ₹65,00,000 per annum (based on experience and qualifications)
About IQVIA:
As a global leader in healthcare data and clinical research, IQVIA integrates science and technology to help life sciences companies accelerate clinical development and bring innovative medical therapies to patients worldwide. Join our cutting-edge pharmacokinetics team to drive meaningful impact in the world of clinical pharmacology.
Apply Now at IQVIA Careers
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