Clinical Pharmacology Lead providing expertise for oncology development programs at Pfizer. Involves planning studies, executing analyses, and regulatory documentation contributions in a hybrid role.
Responsibilities
Join a team of scientists supporting oncology development programs
Act as Clinical Pharmacology Lead providing expertise to a multidisciplinary project team
Provide clinical pharmacology components to Clinical Study Protocols and Reports
Plan, design, and oversee clinical pharmacology studies
Execute appropriate PK/PD analyses and simulations
Recommend clinical doses and dosing regimens in collaboration with relevant groups
Support resolution of clinical pharmacology queries from drug regulatory agencies
Requirements
PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD
0-2 years of post-graduate experience
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)
Benefits
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
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