Position Summary

You will provide clinical and scientific oversight and support for multiple, global Phase 1 - 4 clinical studies in support of the development strategy for programs within the Vaccines portfolio.

Position Responsibilities

• Maintains current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment
• Along with the Lead Clinician, is responsible for the design, scientific oversight, data integrity and quality of the clinical study
• Authors protocols, study level informed consent documents, and contributes to authoring of site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents
• Partners with other clinical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical studies within the assigned program
• Leads clinical input for study setup and design, including data tools, analysis, and database setup
• Contributes to the Statistical Analysis Plan and clinical data outputs
• Reviews and queries study data in support of the clinical data review strategy and collection of quality data and review of emerging clinical data and trends, presents and discusses relevant data to appropriate teams, and other internal/external stakeholders
• In close partnership with medically qualified colleague(s), analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s)
• Follows relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures
• Leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures
• May be a subject matter expert or business process owner for a relevant SOP or procedure

Required Qualifications

• BA/BS Degree in a science or health-related discipline
• A strong clinical research background and Good Clinical Practices experience
• Working experience of vaccines therapeutic area
• Ability to integrate and summarize medical/scientific concepts in protocols and documents
• Proven record of independently writing clinical protocols and study documents
• Experience participating in and informally leading an operational team
• Process improvement experience
• Has working knowledge of statistics, data analysis, and data interpretation
• Exceptional written and oral communication and cross-functional collaborative skills
• Proficient in MS Word, Excel, and PowerPoint

Preferred Qualifications

• MS, Ph

D or Pharm D:

Work Location Assignment

Hybrid

About Pfizer

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

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Equal Employment Opportunity

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Medical

Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.