Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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.