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Research Director Pharmacokinetics

5-7 years
₹38–55 LPA
10 June 13, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Director – Pharmacokinetics
Location: Bengaluru, India (Office-based)
Job ID: R1481439
Job Type: Full Time

About the Role:
IQVIA is seeking a highly experienced Research Director in Pharmacokinetics to lead the planning, analysis, and interpretation of clinical pharmacology data for Phase I-IV studies. This role involves strategic input into study design, regulatory submissions, client consulting, and team mentorship. The ideal candidate brings a deep understanding of PK/PD principles, hands-on analytical skills, and a proven ability to manage and deliver high-impact clinical pharmacology projects.

Key Responsibilities:

Clinical Pharmacology Expertise:

  • Design and oversee clinical pharmacology studies (e.g., dose tolerance, bioavailability, QTc, DDI, and special populations).

  • Analyze and interpret data using noncompartmental and population PK/PD models.

  • Develop protocols, SAPs, and PK/PD deliverables including TLFs and CSR contributions.

Client & Regulatory Engagement:

  • Provide expert consulting to clients and internal teams on study design and development strategies.

  • Prepare and contribute to regulatory submissions including global dossiers and local agency communications.

  • Represent IQVIA in interactions with clients, regulatory bodies, and cross-functional internal teams.

Project Management & Quality Oversight:

  • Ensure timely and high-quality delivery of PK/PD components in clinical projects.

  • Update project managers on deliverables and timelines.

  • Participate in cross-functional teams (e.g., Data Management, CRA, Stats, Programming, Medical Writing).

Team Leadership & Mentorship:

  • Train and mentor junior and new staff in pharmacokinetic principles and project delivery.

  • Lead scientific reviews and implement quality control procedures.

Business Development & Strategy:

  • Contribute to business proposals, budgeting, and client presentations for clinical pharmacology components.

  • Support management in executing strategic initiatives and driving innovation.

Research & Development:

  • Stay updated on advances in PK/PD science through literature, conferences, and professional networks.

  • Apply new technologies and insights to improve study outcomes and operational efficiency.

Qualifications:

  • Ph.D. in Pharmacokinetics, Pharmaceutics, or related field with 5+ years of experience

  • OR Master's/PharmD with 7+ years of experience

  • Strong knowledge of clinical pharmacology principles and current therapeutic landscapes

  • Proficient in WinNonlin, NONMEM, SigmaPlot, SPlus, Microsoft Office, and basic SAS

  • Deep understanding of ICH-GCP and global regulatory frameworks

  • Strong leadership, analytical, and mentoring capabilities

  • Excellent communication, organization, and project management skills

  • Ability to work cross-functionally in a global matrix environment

Estimated Salary: ₹38–55 LPA (based on industry standards for Bengaluru location)

About IQVIA:
IQVIA is a global leader in health information technology and research services, supporting the development of breakthrough therapies and advancing healthcare worldwide. Join us to impact patient lives through science, data, and innovation.