Instagram
youtube
Facebook

Director Pharmacometrics

10+ years
Not Disclosed
10 March 26, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Director Pharmacometrics - West Chester, PA - Teva Pharmaceuticals

Date: March 16, 2025
Location: West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 59973

Who We Are:
Teva Pharmaceuticals is committed to making healthcare affordable and accessible to millions worldwide. Operating in nearly 60 countries, Teva is the world’s leading manufacturer of generic medicines and a producer of many products on the World Health Organization’s Essential Medicines List. Over 200 million people globally take Teva’s medicines daily, and the company continuously strives to expand its impact.

The Opportunity:
Responsible for the design and implementation of PMX strategy at the program level, including constructing, validating, and implementing disease, placebo, exposure-response, and mechanistic PKPD models to evaluate risk/benefit and facilitate drug development decisions, in close collaboration with TS colleagues and other R&D partners.

Essential Duties & Responsibilities:

  • Lead the design and implementation of PMX strategy and other advanced Model-Informed Drug Discovery and Development approaches to enable quantitative decision-making throughout the drug development cycles.

  • Manage and perform pharmacometric analyses internally and through external vendors using various tools and approaches. Integrate, interpret, and report results to project teams and stakeholders.

  • Contribute to key pre-clinical, clinical, and regulatory documents, including clinical study protocols, clinical study reports, modeling reports, investigator brochures, INDs, and BLA/NDAs, ensuring compliance with regulatory requirements.

  • Foster constructive collaboration within drug development teams and with other internal partners (e.g., DMPK, Regulatory Affairs, Clinical Development, and Biostatistics).

  • Monitor timelines, objectives, and budgets, ensuring accuracy and timely communication of high-quality data and results to project teams.

  • Maintain and enhance technical and drug development expertise through training, external meetings, and initiating knowledge-sharing sessions within Teva’s Clinical Pharmacology & Pharmacometrics and other line functions.

  • Act as a technical subject matter expert in clinical pharmacology, DMPK, and pharmacometrics.

  • Attend meetings with internal and external parties, including stakeholders, investigators, outside experts, and health authorities.

Travel Requirements:

  • Ability to travel with overnight stays as required.

Location:

  • Position based out of West Chester, PA, with an option to work from the Parsippany, NJ office.

Your Experience and Qualifications:
Requirements:

  • PhD in Clinical Pharmacology/Pharmaceutical Sciences/Pharmacology/Statistics/Engineering with academic training in Pharmacometrics.

  • Minimum 10 years of hands-on industry experience in Pharmacometrics.

Preference:

  • Experience in more than one therapeutic area and early development.

Technical Knowledge:

  • Strong quantitative skills and expertise (e.g., mechanistic PKPD modeling/systems pharmacology, literature meta-analyses, population modeling, and clinical trial simulations).

  • Excellent knowledge of the drug development process.

  • Strong communication and presentation skills.

Enjoy a More Rewarding Choice:
We offer a competitive benefits package, including:

  • Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment.

  • Retirement Savings: 401(k) with employer match up to 6% and an annual 3.75% Defined Contribution to the 401(k) plan.

  • Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, and holidays.

  • Life and Disability Protection: Company-paid Life and Disability insurance.

The total compensation package may also include additional elements, such as a sign-on bonus, restricted stock units, and discretionary awards, alongside a full range of medical, financial, and other benefits.

Already Working @TEVA?
Current Teva employees should apply through the internal career site available on "Employee Central" for priority consideration.

Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is an equal opportunity employer, providing equal employment opportunities without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity, ancestry, veteran status, national or ethnic origin, or any legally protected status.

Important Notice to Employment Agencies:
Teva Pharmaceuticals does not accept unsolicited assistance from agencies. All CVs/resumes submitted by search firms without a valid written agreement in place will be deemed the sole property of the company.