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Jobs or company...

Director, Clinical Pharmacology

Salary undisclosed
Checking job availability...
Original
Simplified

Must Be On-site 3 Days Per Week in Either East Coast or West Coast Office Locations.

East Coast: New York or New Jersey

West Coast: Alameda County, CA

Excited to partner with one of the most dynamic and innovative biopharmaceutical company is advancing revolutionary technology for Oncology. This company's discovery platform is built on groundbreaking innovations from its founders, including a Nobel Prize winner, along with there leadership members from Merck, Gilead and Bristol-Myers.

The team are seeking a passionate and driven Director of Clinical Pharmacology to join their growing Clinical Development team and contribute to the development of Modeling and Simulation in the Clinical Pharmacology group. The role will focus on various modeling and simulation activities, including NCA, population PK/PD, disease progression, statistical and physiologically-based PK (PBPK) modeling, allometric scaling, quantitative system pharmacology (QSP), clinical trial simulations, literature meta-analysis, machine learning, and other cutting-edge quantitative techniques.

You will also collaborate with Clinical Pharmacology Project Leads, applying quantitative approaches to understand the relationship between drug exposure and response, supporting key decisions such as first-in-human dose selection, RP2D, and labeled dose during regulatory interactions.

This role will require a minimum of three days per week of onsite presence in one of three of the team's office locations, California, New York, or New Jersey, to ensure operational excellence and foster strong collaborations!

Qualifications

  • Extensive hands-on experience with PKPD modeling software (NONMEM, R, SAS, MATLAB, Phoenix, SimCyp, GastroPlus, etc.) is required.
  • Strong knowledge of quantitative pharmacology and significant hands-on experience with PK/PD modeling and simulation to inform dose selection, safety profile characterization, and product labeling.
  • Proven ability to independently plan, organize, and analyze PK/PD data.
  • Highly motivated individual with a strong intellectual and technical background who can thrive in a fast-paced, innovative environment, remaining flexible, proactive, resourceful, and efficient.
  • Excellent problem-solving, written, and oral communication skills.

My client is actively hiring, so please submit or reach out should you be interested in discussing further!

Must Be On-site 3 Days Per Week in Either East Coast or West Coast Office Locations.

East Coast: New York or New Jersey

West Coast: Alameda County, CA

Excited to partner with one of the most dynamic and innovative biopharmaceutical company is advancing revolutionary technology for Oncology. This company's discovery platform is built on groundbreaking innovations from its founders, including a Nobel Prize winner, along with there leadership members from Merck, Gilead and Bristol-Myers.

The team are seeking a passionate and driven Director of Clinical Pharmacology to join their growing Clinical Development team and contribute to the development of Modeling and Simulation in the Clinical Pharmacology group. The role will focus on various modeling and simulation activities, including NCA, population PK/PD, disease progression, statistical and physiologically-based PK (PBPK) modeling, allometric scaling, quantitative system pharmacology (QSP), clinical trial simulations, literature meta-analysis, machine learning, and other cutting-edge quantitative techniques.

You will also collaborate with Clinical Pharmacology Project Leads, applying quantitative approaches to understand the relationship between drug exposure and response, supporting key decisions such as first-in-human dose selection, RP2D, and labeled dose during regulatory interactions.

This role will require a minimum of three days per week of onsite presence in one of three of the team's office locations, California, New York, or New Jersey, to ensure operational excellence and foster strong collaborations!

Qualifications

  • Extensive hands-on experience with PKPD modeling software (NONMEM, R, SAS, MATLAB, Phoenix, SimCyp, GastroPlus, etc.) is required.
  • Strong knowledge of quantitative pharmacology and significant hands-on experience with PK/PD modeling and simulation to inform dose selection, safety profile characterization, and product labeling.
  • Proven ability to independently plan, organize, and analyze PK/PD data.
  • Highly motivated individual with a strong intellectual and technical background who can thrive in a fast-paced, innovative environment, remaining flexible, proactive, resourceful, and efficient.
  • Excellent problem-solving, written, and oral communication skills.

My client is actively hiring, so please submit or reach out should you be interested in discussing further!