Senior Manager – Feasibility Strategic Analytics Lead

Pfizer

. Partner with Clinical Study Team Leads, Participant Recruitment, GSSO roles and Clinical Leads to support predictable delivery of Pfizer’s portfolio .

Posted 9/15/2026full-timeRemote • New York • United StatesSenior💰 $116,000 - $193,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research and drug development, with a strong focus on global country and site feasibility, clinical study start-up, and operational execution. Proven ability to analyze data, develop strategic enrollment plans, and optimize clinical trial processes while maintaining high-quality standards.

Highest-signal resume keywords

Clinical Research ExperienceGlobal Country and Site FeasibilityKnowledge of GCPStrategic Planning and Problem-SolvingOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ConductProgram and Protocol Feasibility AssessmentPatient Volume ModelingEnrollment Strategy DevelopmentData Analysis and Synthesis

Soft Skills

Strong Verbal and Written CommunicationEffective Presentation and FacilitationCustomer Service OrientationAbility to Multitask Under Tight DeadlinesNegotiation and Conflict Moderation

Certifications & Qualifications

BS / RN / MS or PhD / MD

Industry Keywords

Drug DevelopmentClinical Study Start-UpRegulatory OperationsDecentralized Clinical TrialsClinical Trial Diversity Analysis

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Partner with Clinical Study Team Leads, Participant Recruitment, GSSO roles and Clinical Leads to support predictable delivery of Pfizer’s portfolio
Provide rapid, accurate and robust assessments of program and protocol feasibility, recruitment enrollment assumptions and site strategy plans
Build evidence-driven study assumptions and country and site strategies, including proposed countries, sites, enrollment scenarios and protocol optimization strategies
Support study team enrollment strategy through participant recruitment and assess future changes to the strategy
Implement country and site intelligence processes and document changes throughout the study lifecycle
Provide early feasibility assessments, initial enrollment timelines, potential country footprints, intelligence gathering and enrollment assumptions
Introduce protocol optimization opportunities using real-world data, investigator insights, patient insights and protocol simulations
Evolve country footprint, enrollment assumptions and site classification strategy as protocols develop
Support investigator database construction and identify suitable sites and ideal site characteristics
Lead country and site feasibility outreach, engagement and response reviews
Analyze outreach results and evidence to recommend country and site strategies
Provide site analytics, including patient volume modeling, clinical trial diversity analysis, competition and site overlap analysis
Develop strategic scenarios to optimize site footprint and enrollment timelines using internal, external and regional data
Partner with CD&O, RU and BU teams to improve study start-up and recruitment cycle-time metrics
Deliver agreed KPIs for assigned protocols
Promote continuous improvement and adoption of innovative clinical trial technologies
Maintain relationships across platform lines, business/research units and enabling lines
Maintain a portfolio-aligned living library of knowledge and recurring assessments of comparator studies and trial metrics
Analyze program- and indication-level real-world data, standards of care, recruitment rates and disease prevalence
Develop intelligence on preferred sites and evaluate overlapping sites within indications
Analyze decentralized clinical trial applications and recommend appropriate strategies
Evaluate early-stage portfolio assets and partner on internal/external data needs for emerging indications

Requirements

What you’ll need

BS / RN / MS and 7 years relevant experience, or PhD / MD and 3 years relevant experience
Knowledge of drug development and thorough understanding of global country and site feasibility, clinical study start-up and business operations
Experience in clinical research, including clinical trial conduct
Knowledge of GCP
Understanding of study/project management, monitoring, clinical and regulatory operations processes
History of success in a customer service role with demonstration of meeting customer expectations
Strong verbal and written communication skills
Effective presentation and facilitation skills
Strategic planning, observation, analytical operational execution and problem-solving skills
Strong business consultancy skills, including ability to persuade, negotiate and moderate conflict
Ability to multitask under tight deadlines on several projects while maintaining attention to detail and high-quality work
Ability to synthesize key messages across multiple data sets
Experience in operations involving multinational clinical trials preferred
Prior experience in global country and site feasibility preferred
Ability to make complex decisions among multiple options amid competing priorities and ambiguity
Ability to leverage long-term business strategy to prioritize activities and answer key business questions
Oncology experience preferred
Candidates must be authorized to be employed in the U.S. by any employer
Position requires permanent work authorization in the United States
U.S. work visa sponsorship is not available for this role now or in the future

Benefits

Comp & perks

Bonus target of 15.0% 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 assistance may be available based on business needs and/or eligibility