Associate Director, Clinical Pharmacology
$139,100–$231,900 year
HybridNew York City, New York, United States or Cambridge, Massachusetts, United States
Job Summary
Lead clinical pharmacology and model-informed drug discovery (MIDD) for the Internal Medicine portfolio by designing and executing clinical plans, overseeing study-level activities including protocol authoring and phase oversight, and optimizing dose-range finding strategies. Provide expertise to project teams and regulatory interactions while ensuring appropriate preclinical PK/PD knowledge underwrites safe human administration. Plan and interpret PK/PD analyses, biomarker strategies, and End-to-End MIDD plans using innovative analytical methods to integrate pharmacokinetics, pharmacodynamics, and patient characteristics. Coach colleagues, develop new methodologies through external collaborations, and represent the team at scientific societies.
Required Qualifications
- M.D./Ph.D., or equivalent training/experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or related discipline
- Pharm D. or equivalent training/experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or related discipline
- 1+ year Industry experience in clinical pharmacology and/or clinical PK/PD and/or Pharmacometrics/Systems Pharmacology
- 5+ years Industry experience in clinical pharmacology and/or clinical PK/PD and/or Pharmacometrics/Systems Pharmacology
- Intimate knowledge of drug development and experience in applying quantitative pharmacology approaches to knowledge integration
- Excellent written and verbal communication skills
- Demonstrated presentation skills
- Ability to attend global meetings periodically across different time zones
- Candidates must be authorized to be employed in the U.S. by any employer
- U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future
- This position requires permanent work authorization in the United States
- This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed
Desired Qualifications
- Strong quantitative skills and expertise (e.g. experience in mechanistic PK/PD modeling/systems pharmacology, literature meta-analyses, population modeling, and clinical trial simulations using NONMEM, R, etc.)
- Ability to influence and collaborate with peers
- Ability to develop and coach others
- Ability to oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
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