Manager Clinical Pharmacology

ROLE SUMMARY
The candidate will be working in a team of scientists reporting to a group lead in San Diego supporting early and late-stage oncology programs. The candidate will be a part of the Pfizer Oncology Clin Pharm team with approximately 35 scientists. We emphasize on the candidate's quantitative pharmacology skills, scientific reasoning, regulatory affairs skills, written and verbal communication skills, exploratory graphical analysis skills, study design and report writing skills.
The candidate will act as the primary clinical pharmacology lead providing clinical pharmacology expertise to multidisciplinary study teams supporting early and late-stage oncology programs.
"Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact."
ROLE RESPONSIBILITIES

• Provide clinical pharmacology expertise to multidisciplinary study teams for early and late-stage oncology programs.
• Under the supervision of the ClinPharm group leader, work closely with clinicians, statisticians, translational oncology and clinical operations colleagues to design, conduct and report results of clinical trials.
• Responsible for designing and implementing dose finding strategies to ensure optimal dose and dosing regimens in clinical trials.
• Analyze pharmacokinetic data and integrate this knowledge into clinical trial design.
• Draft clinical pharmacology components of protocols, clinical development plans and regulatory documents.

QUALIFICATIONS

• PhD with 0, PharmD with 1 year, OR MS with 3+ years of experience.
• The candidate should have demonstrable skills in quantitative clinical pharmacology, including hands-on implementation of tools such as NONMEM, R, or Monolix for data analysis and handling.
• Effective verbal and written communication skills are essential for the role.
  PHYSICAL/MENTAL REQUIREMENTS
  Sitting, standing, walking, ability to perform mathematical calculations and ability to perform complex data analysis
  NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
  Full time, exempt employee. Some limited business travel.

Work Location Assignment: Hybrid
The annual base salary for this position ranges from $106,000.00 to $171,500.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
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EEO & Employment Eligibility
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.
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