Clinical Development Scientist, Manager--Inflammation and Immunology (I&I)
About The Position
Support the development and execution of one or more less complex studies for small molecule and/or novel biological therapies in the Inflammation and Immunology (I&I) therapeutic area. The role may participate as an individual contributor on clinical study teams, often in partnership with or under the mentorship of a more senior Clinical Development Scientist, supporting enrollment and study delivery timelines. It works with other functional disciplines as needed, including Clinical Operations, Global Clinical Leads/Medical Monitors, Biostatistics/Data Management, Clinical Pharmacology, and Digital Medicine, and may serve on clinical sub-teams to promote collaboration and connectivity across functions. The position is hybrid, with on-site work averaging 2.5 days per week. The employee must live within commuting distance of the site. Relocation support may be available based on business needs and eligibility. Candidates must have permanent authorization to work in the United States; U.S. work visa sponsorship is unavailable.
Requirements
- PharmD or PhD in a related discipline; or MS/MA/MSN and at least 2 years of related industry clinical study experience; or BS/BA/BSN and at least 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.
- Must be authorized to be employed in the U.S. by any employer and have permanent U.S. work authorization; visa sponsorship is not available.
Nice To Haves
- Experience in a clinician-type or clinical operations-type role, including experience executing clinical studies.
- Project Management experience.
Responsibilities
- Support the development and execution of simple to minimally complex clinical studies.
- For more complex studies, support a more senior Clinical Development Scientist by taking responsibility for assigned components of the clinical team's deliverables.
- Support the preparation and review of study-related documents, including clinical protocols, informed consent documents, and study training materials.
- Support clinician data review activities.
- For more complex studies, work with a more senior Clinical Development Scientist to collect and collate safety data for safety review meetings and ongoing monthly data reviews in accordance with the data review plan.
- Provide technical support for clinical issues raised by internal and external collaborators, investigators, consultants, and contractors, in collaboration with the Global Development Lead as needed.
- Collaborate with the study team to maintain open and transparent communication and support successful study completion.
- Work with relevant functional disciplines and participate in clinical sub-teams to support collaboration and connectivity across functions.
Benefits
- 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
- Paid vacation, holidays, and personal days
- Paid caregiver/parental and medical leave
- Medical, prescription drug, dental, and vision coverage
- Eligibility to participate in Pfizer’s Global Performance Plan, with a 15% bonus target of base salary
- Eligibility to participate in a share-based long-term incentive program
- Relocation assistance may be available based on business needs and/or eligibility
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What This Job Offers
Job Type
Full-time
Career Level
Manager
