Pfizer Associate Director, Clinical Pharmacology in La Jolla, California
The candidate will be working in a team of scientists reporting to a group lead in San Francisco supporting a late stage immuno-oncology program. 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 a multidisciplinary study team for a late-stage immuno-oncology program
Provide clinical pharmacology expertise to multidisciplinary study teams for a late-stage immuno-oncology program.
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.
"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."
A clinical pharmacologist with a PhD, Pharm.D (with fellowship) or a MD degree with at least 5-10 yrs. of academic/industry experience.
Ability to apply pharmacokinetic and pharmacokinetic-pharmacodynamic concepts, including the modeling and simulation to clinical trial design.
Strong technical proficiency in pharmacokinetic software (e.g WinNonlin, NONMEM, S+Plus, R, etc.) is preferred.
Proven record in clinical drug development with experience in oncology.
Prior experience with large molecules and/or immuno-oncology or immunology is desirable.
The ideal candidate will be an excellent communicator with strong interpersonal skills
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.
Other Job Details:
Last Date to Apply for Job: 5/23/2020
Additional Location Information: La Jolla, CA
Eligible for Relocation Package
Eligible for Employee Referral Bonus
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