Pharmacokinetic Analyst – Clinical Data focus, Remote Possible

🏢 IQVIA📍 New Port Richey, FL, United States💼 Full-Time💻 Remote🏭 Biotechnology💰 80000-120000 per year

About the Company

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make the greatest positive impact on human health. With a global presence and a diverse team of experts, IQVIA helps clients accelerate drug development and commercialization of innovative medical treatments.

Job Description

We are seeking a highly motivated and detail-oriented Pharmacokinetic Analyst with a strong focus on clinical data to join our dynamic team. This is a remote-first position, offering flexibility and the opportunity to contribute to critical drug development projects from anywhere. The successful candidate will be responsible for conducting pharmacokinetic (PK) analyses, interpreting clinical trial data, and preparing comprehensive reports to support regulatory submissions and internal decision-making processes. This role requires a strong understanding of PK principles, statistical methodologies, and regulatory guidelines.

Key Responsibilities

  • Perform non-compartmental and compartmental pharmacokinetic analyses using specialized software (e.g., Phoenix WinNonlin).
  • Analyze clinical trial data to characterize drug absorption, distribution, metabolism, and excretion (ADME) properties.
  • Interpret PK results in the context of clinical pharmacology and drug development objectives.
  • Develop and validate PK analysis methods and data processing pipelines.
  • Prepare high-quality PK reports, summaries, and presentations for internal teams and external clients.
  • Collaborate with clinical pharmacologists, biostatisticians, and other project team members.
  • Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and standard operating procedures (SOPs).
  • Participate in study design discussions and provide input on PK sampling strategies.
  • Contribute to the development of departmental best practices and training materials.

Required Skills

  • Proficiency in pharmacokinetic software (e.g., Phoenix WinNonlin, R, SAS).
  • Strong understanding of PK/PD principles and modeling techniques.
  • Experience with clinical trial data analysis and interpretation.
  • Excellent written and verbal communication skills.
  • Ability to work independently and collaboratively in a remote team environment.
  • Solid statistical analysis skills.
  • Knowledge of regulatory guidelines (e.g., FDA, EMA) related to PK analysis.

Preferred Qualifications

  • Master's or Ph.D. in Pharmacokinetics, Pharmaceutical Sciences, Biostatistics, or a related field.
  • Experience in a Contract Research Organization (CRO) or pharmaceutical industry setting.
  • Familiarity with population PK analysis (NONMEM).
  • Experience with therapeutic areas such as oncology, immunology, or neuroscience.
  • Publications in peer-reviewed journals related to pharmacokinetics.

Perks & Benefits

  • Comprehensive health, dental, and vision insurance.
  • 401(k) retirement plan with company match.
  • Generous paid time off and holidays.
  • Professional development and training opportunities.
  • Remote work flexibility.
  • Employee assistance program.
  • Life and disability insurance.

How to Apply

If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:

  • An up-to-date Resume or CV
  • A brief cover letter summarizing your experience and motivation

Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.

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