Clinician / Clinical Scientist, Associate Director – Pfizer (Hybrid, North America)
Locations: Any Pfizer Site in North America | Groton, Connecticut | Collegeville, Pennsylvania | New York City, New York
Job Type: Full-Time
Job ID: 4941373
Posted: 11 Days Ago
Position Overview
Pfizer is seeking a highly skilled Clinician / Clinical Scientist, Associate Director to support early-stage clinical research and development across multiple therapeutic programs. This role plays a critical part in advancing small molecule and novel biologic candidates from First-in-Human (FIH) through Proof of Mechanism (PoM), Early Signals of Efficacy (ESoE), and Proof of Concept (PoC).
The Associate Director will collaborate closely with cross-functional teams to ensure high-quality study design, execution, safety monitoring, and data interpretation. Depending on experience, the selected candidate may also lead protocol development and contribute to clinical strategy across assigned projects.
This is a hybrid position, requiring on-site presence for an average of 2.5 days per week.
Key Responsibilities
Clinical and Scientific Leadership
Provide scientific oversight for early clinical studies, ensuring efficient execution and adherence to high-quality standards.
Support or lead development of core study documents, including clinical protocols, informed consent forms, and training materials.
Assist in drafting clinical development plans, investigator brochures, statistical analysis plans, and regulatory documentation.
Study Conduct and Data Evaluation
Perform clinical data review, analysis, and interpretation in partnership with Global Clinical Leads, Clinical Safety, Biostatistics, and Data Management.
Support clinical sub-teams to ensure effective communication and timely study delivery.
Ensure compliance with GCP, regulatory requirements, IRB obligations, and internal Pfizer SOPs.
Cross-Functional Collaboration
Work closely with Clinical Operations, Data Management, Clinical Pharmacology, Digital Medicine, and other relevant partners.
Serve as a technical and scientific resource for internal stakeholders, external collaborators, CROs, and investigators.
Support project teams throughout clinical development milestones and execution of FIH, PoM, ESoE, and PoC trials.
Operational Excellence
Develop proficiency in Pfizer clinical systems including GDMS, pTMF, clinical trial registries, CORD, JReview, and safety signal management tools.
Contribute to process improvements within the Internal Medicine Early Clinical Research group.
Perform additional responsibilities aligned with clinical program needs.
Required Qualifications and Experience
BA/BS/BSN with minimum 4 years of clinical study experience,
or
MA/MBA/MS with minimum 2 years of clinical study experience.
At least 2 years of experience in a clinician-type role with proven success in supporting or executing clinical development programs.
Demonstrated knowledge of early drug development, clinical trial methodology, and adjacent disciplines such as biostatistics, regulatory affairs, clinical pharmacology, and pharmaceutical sciences.
Strong scientific writing, analytical thinking, and communication skills.
Proven ability to collaborate within cross-functional and matrixed environments.
Demonstrated leadership competencies, including the ability to influence, mentor, and guide colleagues.
Organizational Relationships
This role works closely with:
Internal Medicine Early Clinical Research leadership
Global Clinical Leads and Medical Monitors
Biostatistics and Data Management teams
Clinical Operations and Clinical Pharmacology
Digital Medicine
External CROs, AROs, and Data Monitoring Committees
Work Schedule, Travel, and Environment
This is a hybrid role, requiring on-site presence 2.5 days per week.
Travel may be required for investigator meetings and protocol presentations.
Relocation support may be available depending on eligibility and business needs.
Compensation and Benefits
Annual base salary range: USD 135,100 – 225,100
Eligible for Pfizer Global Performance Bonus (17.5% target)
Eligible for long-term share-based incentive program
Comprehensive benefits package including:
401(k) with matching and retirement savings contributions
Paid vacation, holidays, and personal leave
Caregiver, parental, and medical leave
Medical, dental, vision, and prescription coverage
Salary ranges may vary outside the U.S. and exclude Tampa, Florida.
Regulatory and Compliance Notes
Pfizer complies with all federal and state transparency requirements, including the Sunshine Act, which may require reporting of reimbursed expenses for licensed physicians.
Equal employment opportunity is fully upheld, and Pfizer adheres to all applicable employment eligibility verification requirements. Permanent U.S. work authorization is required. Pfizer participates in E-Verify.
How to Apply
Interested candidates may apply through Pfizer’s official career portal.
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