Clinical Development Scientist, Manager – Inflammation and Immunology

Pfizer

. Support the development and execution of simple to minimally complex clinical studies in the inflammation and immunology therapeutic area .

Posted 10/19/2026full-timeUnited StatesJuniorMid-Level💰 $106,000 - $176,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study execution within the inflammation and immunology therapeutic area, with a strong understanding of GCP and ICH guidelines. Proficient in collaborating across multidisciplinary teams to ensure successful study delivery and data management.

Highest-signal resume keywords

Clinical Study ExecutionGCP KnowledgeICH Guidelines FamiliarityMicrosoft Office ProficiencyInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol PreparationSafety Data CollectionData Review SupportStudy Training Material DevelopmentClinical Study Team Participation

Soft Skills

Strong CommunicationInterpersonal Skills

Tools & Technologies

Microsoft WordMicrosoft PowerPointMicrosoft Excel

Industry Keywords

Pharmaceutical EnvironmentBiopharmaceutical EnvironmentDrug DevelopmentClinical OperationsClinical Pharmacology

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the development and execution of simple to minimally complex clinical studies in the inflammation and immunology therapeutic area
Support senior Clinical Development Scientists on assigned components of complex clinical team deliverables
Participate on clinical study teams to support enrollment and study delivery timelines
Collaborate with Clinical Operations, Global Clinical Leads/Medical Monitors, Biostatistics/Data Management, Clinical Pharmacology, Digital Medicine, and other functional disciplines
Participate in clinical sub-teams to ensure collaboration and connectivity across functions
Prepare and review clinical protocols, informed consent documents, and study training materials
Support clinician data review activities
Collect and collate safety data for safety review meetings and ongoing monthly data reviews
Provide technical support for clinical issues raised by collaborators, investigators, consultants, and contractors
Collaborate with study teams to maintain communication and support successful study completion

Requirements

What you’ll need

PharmD/PhD in a related discipline OR MS/MA/MSN and 2+ years of related industry clinical study experience OR BS/BA/BSN and 4+ years of related industry clinical study experience
Comprehensive knowledge of GCP and ICH guidelines
Good understanding of the pharmaceutical/biopharmaceutical environment and drug development
Strong communication and interpersonal skills
Proficiency in Microsoft Office applications, including Word, PowerPoint, and Excel
Candidates 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

Relocation support may be available based on business needs and/or eligibility
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
Participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary
Eligibility to participate in Pfizer’s share based long term incentive program