21 час назад
Associate Director, Clinical Pharmacology
139 100 - 231 900$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Director, Clinical Pharmacology (MIDD): Leading clinical pharmacology and model-informed drug development plans for Pfizer’s Internal Medicine portfolio with an accent on PK/PD modeling, dose optimization, and regulatory strategy. Focus on designing clinical studies, integrating patient and disease data into predictive models, and guiding cross-functional teams through drug development decisions.
Location: New York City, United States; hybrid role requiring residence within commuting distance and on-site work an average of 2.5 days per week or more as needed.
Annual base salary: $139,100–$231,900, plus a 17.5% bonus target and eligibility for a share-based long-term incentive program.
Company
is a pharmaceutical company developing medicines through clinical research and model-informed drug development.
What you will do
- Represent Clinical Pharmacology on clinical sub-teams, development teams, and other multifunctional project teams.
- Design and execute clinical pharmacology plans and deliverables for Internal Medicine projects.
- Plan and oversee PK/PD analyses, immunogenicity and biomarker strategies, study protocols, clinical phase activities, and reporting.
- Develop dose-ranging strategies and optimize doses, dosage regimens, and study designs using quantitative pharmacology.
- Lead end-to-end MIDD plans and contribute to regulatory documents, including IND, NDA/MAA, investigator’s brochures, briefing documents, and regulatory responses.
- Develop new methodologies, collaborate with external experts, coach colleagues, and represent the field through publications and presentations.
Requirements
- MD, PhD, PharmD, or equivalent training and experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or a related discipline.
- At least 5 years of industry experience in clinical pharmacology, clinical PK/PD, pharmacometrics, or systems pharmacology.
- Strong quantitative expertise in mechanistic PK/PD modeling, systems pharmacology, population modeling, literature meta-analyses, and clinical trial simulations.
- Experience with NONMEM, R, or comparable quantitative pharmacology tools.
- Knowledge of drug development and quantitative approaches to knowledge integration, along with strong written, verbal, and presentation skills.
- Permanent authorization to work in the United States is required; U.S. work visa sponsorship is not available now or in the future.
Nice to have
- Experience developing methodologies through collaboration with external experts and scientific organizations.
- Ability to attend global meetings periodically across different time zones.
Culture & Benefits
- Hybrid work arrangement with regular on-site collaboration.
- Comprehensive medical, prescription drug, dental, and vision coverage.
- 401(k) plan with matching contributions and an additional retirement savings contribution.
- Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
- Relocation assistance may be available based on business needs and eligibility.
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