Senior Manager – Feasibility Strategic Analytics Lead

This is a fully remote position, open to applicants in New York.

📋 Description

• Collaborate with Clinical Study Team Leads, Participant Recruitment, GSSO roles, and Clinical Leads to ensure reliable delivery of Pfizer’s portfolio.

• Deliver swift, precise, and comprehensive evaluations of program and protocol feasibility, recruitment enrollment forecasts, and site strategy plans.

• Develop evidence-based study assumptions and strategies for countries and sites, incorporating proposed countries, sites, enrollment scenarios, and protocol optimization approaches.

• Assist the study team in forming enrollment strategies through participant recruitment and evaluate any future modifications to the strategy.

• Implement processes for country and site intelligence and document any changes throughout the study's lifecycle.

• Provide preliminary feasibility assessments, initial enrollment timelines, potential country footprints, intelligence gathering, and enrollment assumptions.

• Identify opportunities for protocol optimization by utilizing real-world data, insights from investigators, patient feedback, and protocol simulations.

• Adapt country footprints, enrollment assumptions, and site classification strategies as protocols evolve.

• Aid in constructing an investigator database and identifying suitable sites along with their ideal characteristics.

• Lead outreach efforts for country and site feasibility, engagement, and response evaluations.

• Analyze outreach outcomes and evidence to recommend strategies for countries and sites.

• Provide site analytics, which includes patient volume modeling, clinical trial diversity analysis, and competition and site overlap analysis.

• Develop strategic scenarios aimed at optimizing site footprints and enrollment timelines using both internal and external regional data.

• Collaborate with CD&O, RU, and BU teams to enhance study start-up and recruitment cycle-time metrics.

• Achieve agreed KPIs for designated protocols.

• Advocate for continuous improvement and the adoption of innovative technologies in clinical trials.

• Maintain relationships across various platform lines, business/research units, and enabling lines.

• Keep a portfolio-aligned living library of knowledge and ongoing assessments of comparator studies and trial metrics.

• Analyze real-world data at the program and indication levels, alongside standards of care, recruitment rates, and disease prevalence.

• Gather intelligence on preferred sites and assess overlapping sites within indications.

• Examine decentralized clinical trial applications and suggest suitable strategies.

• Evaluate early-stage portfolio assets and collaborate on internal/external data requirements for emerging indications.

⛳️ Requirements

• BS / RN / MS with 7 years of relevant experience, or PhD / MD with 3 years of relevant experience.

• Proficient understanding of drug development, alongside a comprehensive grasp of global country and site feasibility, clinical study start-up, and business operations.

• Experience in clinical research, particularly in clinical trial execution.

• Familiarity with GCP.

• Understanding of study/project management, monitoring, clinical, and regulatory operations processes.

• Proven success in a customer service role, demonstrating the ability to meet customer expectations.

• Excellent verbal and written communication skills.

• Strong presentation and facilitation abilities.

• Competence in strategic planning, observation, analytical operational execution, and problem-solving.

• Solid business consultancy skills, including the capacity to persuade, negotiate, and mediate conflicts.

• Capacity to handle multiple projects under tight deadlines while maintaining attention to detail and high-quality output.

• Ability to distill key messages from various data sets.

• Experience in operations related to multinational clinical trials is preferred.

• Prior experience in global country and site feasibility is advantageous.

• Ability to make intricate decisions among diverse options amid competing priorities and uncertainties.

• Capability to leverage long-term business strategies to prioritize activities and address key business inquiries.

• Experience in oncology is preferred.

• Candidates must be eligible to work in the U.S. for any employer.

• The position necessitates permanent work authorization in the United States.

• U.S. work visa sponsorship is not available for this role, now or in the future.

🏝️ Benefits

• 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, holidays, and personal days.

• Paid caregiver/parental and medical leave.

• Comprehensive medical, prescription drug, dental, and vision coverage.

• Relocation assistance may be available based on business needs and/or eligibility.