Research Director Pharmacokinetics

IQVIA; Reading; On-site; GBP 50,000 - 80,000; Full time

Job summary

IQVIA is seeking a Research Director in Pharmacokinetics to lead analysis and reporting of clinical pharmacology studies. This role involves consulting on study design, preparing regulatory submissions, and mentoring junior staff, requiring advanced degrees and significant experience in pharmacokinetics.

Qualifications

• 5-7 years experience in pharmacokinetics required.
• Sound knowledge of current therapeutic environment and drug development trends.
• Good problem solving and analytical skills are essential.

Responsibilities

• Perform analysis and reporting of Phase I-IV clinical pharmacology studies.
• Consult on study design and prepare global dossiers for product registration.
• Provide technical training and mentorship to lower level and new staff.

Skills

Pharmacokinetic concepts

Problem solving

Analytical skills

Coaching and mentoring

Verbal communication

Written communication

Education

Ph.D. or educational equivalent in Pharmacokinetics

Master's Degree or PharmD in Pharmacy

Tools

Microsoft Office

WinNonlin

SigmaPlot

NONMEM

SPlus

SAS programming

Job description

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Research Director Pharmacokinetics, Reading

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Client:

IQVIA

Location:

Reading, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

1c429cd87df3

Job Views:

4

Posted:

29.06.2025

Expiry Date:

13.08.2025

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Job Description:

Job Overview
Perform analysis and reporting of Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies. Provide consulting on study design, or other aspects of Clinical Pharmacology projects, clinical development plans, and dossiers for product registration. Assist Clinical Pharmacology management in implementing strategic initiatives.

Essential Functions
• As a project PK Scientist develop or oversee the development of protocols, statistical analysis plans, PK/PD analysis, PK/PD tables, listings and figures, and clinical study reports for Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies.
• Consult with clients, external IQVIA divisions, and Clinical Pharmacology staff on study design, or other aspects of Clinical Pharmacology projects, and clinical development plans.
• Prepare PK/PD sections of global dossiers for product registration and communicate with local regulatory agencies.
• Ensure quality and timely delivery of the project PK/PD deliverables to IQVIA clients.
• Provide update to the IQVIA Project Manager on status of project PK/PD deliverables.
• Participate on project-related cross functional teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer.
• Consult and interact with clients, other IQVIA divisions, and third-party vendors.
• Provide technical training, guidance, and mentorship to lower level and new staff.
• Participate in proposal and budget development for Clinical Pharmacology PK/PD components of business proposals.
• Recommend and assist in implementation of quality control (QC) assessment and procedures and scientific review.
• Assist management in implementing strategic initiatives.
• Maintain awareness of overall developments in the field of Clinical Pharmacology and PK/PD based on current literature, application of new technology, attendance at professional meetings, etc.
• Perform other duties as assigned by Clinical Pharmacology Management.

Qualifications
• Ph.D. or educational equivalent in Pharmacokinetics, Pharmaceutics, or related field Req Or
• Master's Degree or PharmD in Pharmacy or related field Req
• 5 years experience Req Or
• 7 years experience Req Or
• Equivalent combination of education, training and experience Req
• Sound knowledge of Pharmacokinetic concepts, including noncompartmental analysis and population PK modeling as required, current therapeutic environment and drug development trends
• Sound knowledge of appropriate PK/PD standards and processes
• Strong understanding of the principles of the drug development process, ICH GCP, and applicable International and national regulatory requirements
• Good coaching and mentoring skills
• Good problem solving and analytical skills
• Excellent computer skills, including proficiency with Microsoft Office, WinNonlin, and SigmaPlot graphics, as well as NONMEM, SPlus and basic SAS programming, as required
• Excellent verbal and written communication skills and highly effective interpersonal, and organizational skills
• Ability to work within a matrix team environment
• Ability to prioritize, and independently coordinate and manage PK/PD component of complex projects
• Ability to interact in a cross-functional and multi-cultural team environment
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at