Impress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now

About the Role

Will join a team of scientists supporting oncology development programs. Will be the Clinical Pharmacology Lead providing clinical pharmacology expertise to a multidisciplinary project team of an oncology program.

Responsibilities

• Acts as Clinical Pharmacology representative on Clinical Sub Team and Development Team.
• Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports, and Clinical Pharmacology plans for programs.
• Provides clinical pharmacology expertise to oncology project teams, including planning, design, and oversight of clinical pharmacology studies.
• Participates in implementing model-based drug development using quantitative approaches.
• Provides non-compartmental analysis of PK data and executes appropriate PK/PD analyses such as population PK modeling, PK/PD modeling, and conducting simulations.
• Plans relevant PK/PD analyses and integrates knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and disease states to optimize doses and dosage regimens.
• Provides recommendations for clinical doses and dosing regimens to Clinical and Development teams and in regulatory documentation.
• Responsible for clinical pharmacology contributions to all regulatory documents, including Investigator Brochures and EOP2 meetings.
• Supports the resolution of clinical pharmacology queries from drug regulatory agencies and leads the writing and review of responses.
• Works in a matrix environment with a cross-functional clinical team.

Requirements

• PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD
• Strong written and verbal communication skills
• Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial and overall clinical program.
• Hands-on experience with common software tools for PK and PK/PD analyses (e.g., R, NONMEM, Monolix)
• Candidates must be authorized to be employed in the U.S. by any employer.
• U.S. work visa sponsorship is not available for this role now or in the future.

Skills

• Clinical Pharmacology
• Oncology
• PK/PD modeling
• Population PK modeling
• Simulations
• R
• NONMEM
• Monolix

Location

• Flexible
• Hybrid

Work Type

• Hybrid

Experience Level

• Clinical Pharmacology Lead

Education Level

• PhD
• PharmD

Salary/Compensations

• $106,000.00 - $176,600.00
• 15.0% bonus target

Benefits

• Relocation support available
• 401(k) plan with Pfizer Matching Contributions
• Additional Pfizer Retirement Savings Contribution
• Paid vacation, holiday, and personal days
• Paid caregiver/parental and medical leave
• Health benefits including medical, prescription drug, dental, and vision coverage

About the Company

• Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws.
• Pfizer endeavors to make www.pfizer.com/careers accessible to all users.

Equal Opportunity

• Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.
• Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.
• Pfizer is an E-Verify employer.
• This position requires permanent work authorization in the United States.