Clinical Development Scientist, Director – Inflammation and Immunology

Pfizer

. Lead and coordinate development of multiple clinical studies for novel biologic and small molecule therapies across clinical development stages .

Posted 10/19/2026full-timeUnited StatesLead💰 $176,600 - $294,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical development and research, with a strong focus on protocol development, data analysis, and regulatory compliance. Proven ability to lead cross-functional teams and communicate effectively with stakeholders at all levels.

Highest-signal resume keywords

Clinical Development LeadershipScientific WritingData AnalysisRegulatory ComplianceCross-Functional Team Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol DevelopmentClinical Data ReviewBiostatisticsClinical PharmacologyDrug DevelopmentSafety AssessmentsStatistical AnalysisClinical ResearchBiopharmaceutical KnowledgeInformed Consent Development

Soft Skills

Verbal CommunicationPresentation SkillsInfluencing StakeholdersBuilding ConsensusCoaching Others

Tools & Technologies

Pfizer Compliance SystemsStudy SystemsClinical Trial Registries

Certifications & Qualifications

PhDPharmD

Industry Keywords

Good Clinical PracticeClinical OperationsTherapeutic AreasClinical Study DesignRegulatory Affairs

About the role

Key responsibilities & impact

Lead and coordinate development of multiple clinical studies for novel biologic and small molecule therapies across clinical development stages
Lead clinical protocol development and participate as an individual contributor on clinical study teams
Provide scientific leadership for clinical study design, execution, interpretation, safety assessments, and clinically meaningful outcomes
Lead and support clinical development programs within project teams
Serve as a technical resource for internal and external collaborators, investigators, consultants, and contractors
Support publications, abstracts, presentations, and scientific communications
Support clinical development strategy, study implementation, and key milestones including study startup, conduct, and delivery
Lead preparation of clinical protocols and contribute to informed consent forms, training materials, investigator brochures, statistical analysis plans, and regulatory documents
Lead clinical data review, including collection, analysis, and interpretation of safety and efficacy data
Collaborate with study teams to support successful study execution and completion
Develop partnerships with cross-functional Pfizer teams including Biostatistics, Regulatory Affairs, Clinical Pharmacology, and Clinical Operations
Manage priorities across project teams, core study teams, and clinical sub-teams
Ensure compliance with Good Clinical Practice, regulatory requirements, Institutional Review Boards, and Pfizer standards
Use Pfizer compliance systems, registries, and study systems to improve study execution
Incorporate biomarker strategies into therapeutic area programs
Maintain relationships with external experts, consultants, key opinion leaders, regulators, and investigator networks
Maintain current knowledge of scientific and clinical literature relevant to I&I therapeutic areas

Requirements

What you’ll need

PhD/PharmD and 5+ years of relevant industry experience in clinical development, clinical research, or a related drug development role, with a demonstrated track record of supporting development programs through key milestones OR MS and 7+ years of relevant industry experience OR BSc and 8+ years of relevant industry experience
Deep understanding of the biopharmaceutical environment and clinical drug development
Familiarity with Biostatistics, Regulatory Affairs, Clinical Pharmacology, and Pharmaceutical Sciences
Experience developing and coaching others, guiding cross-functional teams, and driving meaningful business impact
Strong scientific writing, presentation, and verbal communication skills
Experience building consensus, influencing stakeholders, and driving change across all levels of the organization, including senior leadership
Strong experience reviewing clinical data listings and interpreting study data
Ability to perform complex data analysis
Occasional travel of 5–10%
Must be authorized to be employed in the U.S. by any employer
Permanent work authorization in the United States required
U.S. work visa sponsorship is not available now or in the future

Benefits

Comp & perks

Bonus target of 20.0% of base salary through Pfizer’s Global Performance Plan
Eligibility to participate in Pfizer’s share based long term incentive program
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Medical, prescription drug, dental and vision coverage
Relocation support may be available
Relocation assistance may be available based on business needs and/or eligibility