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Associate Director - Pharmacokinetics, Dynamics, and Metabolism (PKDM) - HYBRID - $175,000 to $210,000
Cambridge, MA · $175,000 to $210,000OPEN JOB: Associate Director - PKDM
LOCATION: Candidate can choose either Cambridge Mass or Bridgewater NJ
SALARY: $175,000 to $210,000
FULL-TIME
BENEFITS - Full
RELOCATION ASSISTANCE AVAILABLE
REQUIREMENTS:
If you are interested in pursuing this opportunity, please respond back and include the following:
Upon receipt, one of our managers will contact you to discuss the position in full detail.
JASON DENMARK
Recruiting Manager
INTERMEDIA GROUP, INC.
EMAIL: jdenmark@intermediagroup.com
LINKEDIN: https://www.linkedin.com/in/jasondenmark/
LOCATION: Candidate can choose either Cambridge Mass or Bridgewater NJ
- Flexible work from home days
- hybrid schedule, 50% of time must be in the office
SALARY: $175,000 to $210,000
FULL-TIME
BENEFITS - Full
RELOCATION ASSISTANCE AVAILABLE
- The Pharmacokinetics, Dynamics, and Metabolism (PKDM) department at the company contributes to the safe and effective therapeutic treatment of each patient by applying appropriate pharmacokinetic (PK) and pharmacodynamic (PD) principles to drug development and accelerating the process, where possible. PKDM generates, integrates, and leverages clinical and non-clinical PK, PK/PD and metabolism knowledge to support critical decision making and risk management for projects from first in human dosing through life cycle management. As such, we aid in dose selection/study design, de-risking of drug-drug interactions, benefit/risk assessment, and formulation development, with the use of Population PK, PK/PD, and PBPK approaches as appropriate, and contribute to regulatory submissions/interactions.
- PKDM at the company is seeking a dynamic individual to serve as a PK/PD expert participating in multidisciplinary teams for clinical phase development projects in different therapeutic areas. This position will be based in Cambridge, MA.
- Serves as a PKDM representative on project team(s) and works in close collaboration with multidisciplinary team to progress drug candidates from IND through early phase/late phase to successful approval.
- Responsible for the design, planning and oversight of relevant studies, as well as PK/PD analysis, interpretation, and reporting of results for molecules/compounds in clinical stage.
- Applies quantitative skills, via modeling and simulation, to provide dose selection and complex issues at various stages of drug development.
- Responsible for clinical pharmacology contributions to regulatory documents and inquiries.
- Interfaces with Research and works closely with discovery research during the pre-IND stages of drug development to ensure sufficient PK/PD knowledge exists for translation to the clinic.
REQUIREMENTS:
- MS/MA degree in fields listed above plus at least 12 years of relevant experience -OR- Ph.D. degree in clinical pharmacology, pharmacokinetics, pharmacometrics, mathematics, engineering, computational biology or a related field required, with or without post-doctoral experience plus 5 years of relevant experience,
- Minimum 5 years of experience in clinical PK/PD, pharmacometrics, and/or clinical pharmacology
- Must have HANDS ON MODELING experience Proficient in PK modeling software/platforms.
- Effective communication and interpersonal skills.
- Strong presentation skills
- Collaborative team player.
If you are interested in pursuing this opportunity, please respond back and include the following:
- MS WORD Resume
- required compensation.
- Contact information.
- Availability
Upon receipt, one of our managers will contact you to discuss the position in full detail.
JASON DENMARK
Recruiting Manager
INTERMEDIA GROUP, INC.
EMAIL: jdenmark@intermediagroup.com
LINKEDIN: https://www.linkedin.com/in/jasondenmark/