Incyte

Associate Director, Quantitative Pharmacology

Incyte$130K — $160K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, Engineering, or a related field.
  • 3-5 years of industry experience.
  • Proficiency in statistical programming languages and pharmacometrics analysis software including R and NONMEM.
  • Strong communication skills for collaboration with cross-functional teams.
  • Effective time management to handle multiple tasks for program goals.

Responsibilities

  • Conduct and report model-based analyses including population pharmacokinetics (PK) and pharmacokinetics/pharmacodynamics (PK/PD).
  • Identify opportunities to leverage modeling and simulation across multiple projects.
  • Develop MIDD strategies to optimize studies and inform clinical development and regulatory strategies.
  • Communicate pharmacometrics analysis results to influence decision-making.
  • Mentor peers in pharmacometrics methodologies and application in drug development.
  • Stay informed on scientific advancements and regulatory trends in clinical pharmacology and pharmacometrics.
  • Publish findings in peer-reviewed journals.

Benefits

  • Opportunity for professional growth in a leading organization.
  • Engagement in innovative drug development projects.
  • Collaborative work environment with cross-functional teams.
  • Access to current scientific advancements and regulatory trends.
  • Potential for contributing to publications in peer-reviewed journals.
Full Job Description
Overview

Job Summary (Primary function)

We are seeking a pharmacometrician to join our Clinical and Quantitative Pharmacology organization in Translational Medicine. An Associate Director is responsible for executing on the pharmacometrics strategy and model-based analyses for clinical drug development and is expected to play a key role in supporting programs. This role will be responsible for developing and implementing model-informed drug development (MIDD) strategies to optimize decision-making across all phases of drug development.

Essential Functions of the Job (Key responsibilities)
  • Responsible for independently conducting and reporting model-based analyses including population pharmacokinetics (PK) and pharmacokinetics/pharmacodynamics (PK/PD), exposure-response modeling, model-based meta-analyses (MBMA), disease progression modeling, and clinical trial simulation.
  • Identifies opportunities where modeling and simulation can advance the understanding of pharmacokinetics, pharmacodynamics, efficacy, and safety across multiple projects
  • Accountable for developing MIDD strategies across multiple programs and disease areas to optimize prospective studies, inform the overall clinical development and regulatory strategies in collaboration with partners (clinical pharmacology, biostatistics, regulatory, and clinical development teams)
  • Effectively communicates results, conclusions, and assumptions of pharmacometrics analyses to a variety of audiences to influence the decision-making process (written and oral presentation)
  • Mentors and guides peers in pharmacometrics methodologies, tools, and their application in clinical drug development
  • Stays current with scientific advancements and regulatory trends in clinical pharmacology and pharmacometrics, and applies the knowledge to advance drug development for the organization
  • Publishes in peer-reviewed journals

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Ph.D. in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, Engineering, or a related field.
  • Demonstrated 3-5 years of related industry experience.
  • Hands-on experience in a statistical programming language and pharmacometrics analysis software including R and NONMEM or equivalents
  • Excellent communication skills and ability to collaborate with cross-functional teams
  • Time management and ability to balance execution of multiple tasks to accomplish program goals.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

About Incyte

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of proprietary therapeutics. The company was founded in 1991 and is headquartered in Wilmington, Delaware. Incyte's main focus is on oncology, inflammation, and autoimmunity. The company's flagship product, Jakafi, is a JAK1/JAK2 inhibitor used to treat myelofibrosis and polycythemia vera. Incyte has a number of other products in development, including itacitinib, a JAK1 inhibitor for the treatment of graft-versus-host disease, and pemigatinib, a FGFR inhibitor for the treatment of cholangiocarcinoma.
Learn more about Incyte
Size
2,094 employees
Market Cap
$17.6 billion
Industry
Net Income
-$295.7 million
Founded
1991
5 Year Trend
+22%
Revenue
$2.6 billion
NASDAQ

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