Senior Manager – Feasibility Strategic Analytics Lead

🔥 13 hours ago

🗽 New York – Remote

🗽 New York – Remote

💵 $116k - $193.4k / year

⏰ Full Time

🟠 Senior

📊 Data Scientist

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• 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

• 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

• 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