You will provide medical and scientific leadership for one or more complex clinical trials within our Inflammation and Immunology portfolio. You will be responsible for the clinical integrity, scientific quality, and patient safety of clinical studies, partnering closely with Clinical Operations and cross-functional stakeholders to deliver high-quality, efficient trials.
You will play a critical role in protocol development, study execution, data interpretation, and risk management, while serving as the primary clinical contact for investigators and internal study teams.
In addition, you will drive the integration of AI-enabled and advanced analytics solutions to transform clinical development workflows, improving speed, efficiency, and decision-making across the clinical trial lifecycle.
Core Clinical Leadership
Lead the clinical execution of one or more medium- to high-complexity clinical studies
Provide clinical leadership in protocol design and development
Partner with Clinical Operations and cross-functional teams
Oversee clinical data review and safety surveillance
Serve as the primary clinical contact for stakeholders
AI-Enabled Clinical Development & Innovation
Lead identification and implementation of AI/ML and advanced analytics tools to optimize clinical trial design and execution]
Partner with Data Science, Digital, and Technology teams to translate AI use cases into scalable workflows
Champion adoption of innovative tools across study teams
Clinical Strategy and Deliverables
Contribute to clinical documents (protocols, CSRs, regulatory submissions)
Support risk management and safety review
Incorporate AI-derived insights and data-driven approaches into clinical strategy and regulatory deliverables where appropriate
MINIMUM QUALIFICATIONS
PhD/Pharm D in a relevant Science discipline and minimum of 5 years Clinical Research experience in the biopharmaceutical industry, OR
MS in a relevant Science discipline and minimum of 7 years of Clinical Research experience in the biopharmaceutical industry OR
BA/BS in a relevant Science discipline and minimum of 8 years Clinical Research experience in the biopharmaceutical industry
Deep knowledge of clinical development, ICH/GCP, global regulatory requirements, and safety management
Experience leading complex clinical studies and working effectively in cross‑functional, global teams
Strong written and verbal communication skills, with experience engaging internal and external stakeholders
Experience applying AI, machine learning, or advanced analytics in clinical development or research (e.g., protocol design and optimization, site selection and feasibility assessment, query management and workflow automation, data cleaning, anomaly detection, and signal identification, safety risk prediction and proactive mitigation)
Familiarity with AI-enabled use cases including protocol design, recruitment optimization, data review, and safety prediction
Experience partnering with data science or digital teams
Understanding of data governance and AI considerations in GxP environments
PREFERRED QUALIFICATONS
Advanced degree or professional certification in a scientific, medical, or healthcare related discipline
Experience in respiratory and/or dermatology therapeutic areas
Experience with real-world data, digital endpoints, or innovative clinical technologies
COMPETENCIES FOR SUCCESS
Promotes innovation and challenges the status quo
Embraces evolving technologies
Demonstrates intellectual curiosity and proactively explores emerging tools (including AI) to continuously improve and transform clinical development workflows
Demonstrates digital and data fluency, with ability to leverage AI tools responsibly and effectively
Balances innovation with patient safety, regulatory compliance, and scientific rigor
Demonstrates strong judgment and decision-making
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
PHYSICAL/MENTAL REQUIREMENTS
None
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Occasional travel may be required
Relocation support available
WORK LOCATION ASSIGNMENT: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
Work Location Assignment: Hybrid
Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Sunshine Act
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EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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Medical