Senior Director, Oncology Pipeline
CurrentHTA Value & Evidence Lead, breast cancer and early development programs.
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@pfizer.com
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Kristina Chen is listed as Global Access Value - Oncology Precision Medicine at Pfizer, based in Cambridge, Massachusetts, United States. AeroLeads shows a work email signal at pfizer.com and a matched LinkedIn profile for Kristina Chen.
Kristina Chen previously worked as Senior Director, Oncology Pipeline at Pfizer and Director, Global Access Value - Value & Evidence at Pfizer. Kristina Chen holds Master Of Science (M.S.), Pharmaceutical Economics And Policy from University Of Southern California.
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Pharmaceutical Economics Professional with demonstrated expertise in health economic, outcomes research, and epidemiology (HEORE) to generate evidence to support commercialization of oncology/hematology and rare disease products. Scope of work includes: leading products and global product strategy, developing evidence generation plans, devising study designs, implementing, and managing HEORE studies to generate key HEORE evidence to support market access and tools for the medical liaison team; contributing to development of value strategy for multiple stakeholders (patients, payers, and clinicians), working with internal stakeholders (clinical development, commercial and payer teams) to align product goals and value propositions, identifying necessary HEORE projects at different stages of a product’s life cycle, publishing/presenting research results in peer-reviewed journals at large professional congresses and across multiple functions within an organization. Scope of work includes: Leading products and value strategies, developing evidence generation plans, devising product investment portfolio, aligning product value propositions across multiple functions, identifying PRO clinical trial endpoints and devising analysis plans, managing projects and budgets, writing proposals, reports and manuscripts, developing models, analyzing data, deriving conclusions, publishing/presenting research results in peer-reviewed journals, at large professional congresses and across multiple functions within an organization. Key competencies include:• Product lead• Product value and strategy planning• Quantitative analytical skills • Economic modeling • Retrospective claims & EMR Database Analysis• Patient reported outcomes (PRO) instrument development • Project management• Verbal and written ommunication of strategies, research plans and results
Listed skills include Health Economics, Data Analysis, Outcomes Research, Clinical Research, and 12 others.
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New York, New York, Us
HTA Value & Evidence Lead, breast cancer and early development programs.
New York, New York, Us
Global health economics and outcomes research, rare diseases and early pipeline
San Diego, Ca, Us
Product lead, development in value access strategy, patient- reported outcomes (PRO), real world evidence, decision and economic modeling
Tokyo, Jp, Jp
Lead multiple products with rare diseases indications. Provide global strategy input for development of product value propositions. Strategically device evidence generation plan for each products based on product’s stage in life cycle, clinical benefits and comparative edge of the products. Execute evidence generation plans with rigorous scientific research process and analytical methods to support product values and gain market access for the products globally. Work with Global Market Access to generate evidence to support submissions to various health technology assessment (HTA) agencies outside of US. • Lead and contribute to global product strategies and align with the goals among members of the Global Development Team (GDT) (clinical and medical teams) and Global Value Team (GVT) (commercial, market access, clinical, etc.) for rare disease business unit • Support development and implementation of GHEORE studies in the product strategy agreed upon by GVT to demonstrate the values of Shire’s products to key stakeholders (patients, clinicians and payers)• Provide support on current research methods, tools and data sources to ensure study designs and data interpretations are technically accurate and appropriate for market access, commercialization and publication needs• Engaging cross functional team members of the products and effectively executing strategy via internal teams and external consultants• Execute product evidence generation plans and managing all research projects to meet GHEORE product goals set with cross functional teams• Effectively communicate strategy input, GHEORE product goals, study designs and analytical plans, and results to cross functional teams • Disseminate study results internally at key cross functional team meetings (product strategy team and GDT) and externally at key clinical congresses and manuscript publications
Provided consultation to clients for their business needs in market access• Developed proposals and study protocols for evidence generation to understand areas of unmet needs in current treatment for type 1 and type 2 diabetes mellitus using real world data• Devised study analytical plans for retrospective data analyses using electronic medical record databases from global settings (e.g. US, Germany) to generate evidence to support client’s needs in global market access
Thousand Oaks, Ca, Us
Worked on an oncology supportive product and a pipeline product in neuroscience. Collaborated with Global Health Economics product teams to devise product portfolio investment plan and communicate plan to cross-functional teams including clinical, commercial, market value access and payers functions. Assisted alignment of goals for supporting product value propositions across functions. • Updated and developed value propositions for a cancer supportive product.• Interacted with Medical Communications to provide product value messages and supporting data for preparation of materials to support regional field staff.• Communicated with Medical Writing to update existing dossier and align dossier content with value messages. • Developed and managed research projects to provide clinical and economics evidence to support medical, commercial and market value access goals.• Collaborated with Clinical Development team to identify PRO trial endpoints and devise analytical plans in phase II for small-cell lung cancer • Developed a disease specific patient reported outcomes instrument in accordance with FDA guidelines to support labeling claim.• Managed in content development phase of a patient-reported-outcome instrument development for a pipeline product.
Boston, Ma, Us
Developed proposals, estimated project budgets, devised analysis plans and provided case management for multiple case types including large claims data analyses, health economics models, pharmacovigilance using MedWatch™ and Vigibase™ databases, prospective patient surveys, and medical chart reviews. • Managed projects, delegated project tasks, managed project budgets and timelines, and analyzed data. Communicated, analysis plans and project results to clients. • Developed Markov cost-effectiveness models, budget impact models, and early phase pricing models for oncology products for treatment of multiple myeloma and lung cancer• Devised analysis plans for a patient chart review study and analyzed data for products in renal carcinoma • Coordinated and collaborated with both internal and external case members and external vendors to develop electronic case reporting form for chart review. • Collaborated with numerous clinics for participation in chart review studies and presented projects at various professional and clinical conferences. • Developed and submitted manuscripts for publication in peer-reviewed journals.
Developed health economic models and budget impact models using MS Excel®. Devised strategic planning in research and analysis plans for clients’ products throughout various development stages and post-marketing. • Provided consultation on the economic endpoints for Phase II and III clinical trials. • Developed product dossiers to help clients communicate their product values to health care decision makers. • Presented projects at various conferences.
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Kristina Chen works for Pfizer.
Kristina Chen is listed as Global Access Value - Oncology Precision Medicine at Pfizer.
AeroLeads has found 1 work email signal at @pfizer.com for Kristina Chen at Pfizer.
Kristina Chen is based in Cambridge, Massachusetts, United States while working with Pfizer.
Kristina Chen has worked for Pfizer, Arena Pharmaceuticals, Inc., Takeda, Shire, and Independent Consulting, Health Economics.
You can use AeroLeads to view verified contact signals for Kristina Chen at Pfizer, including work email, phone, and LinkedIn data when available.
Kristina Chen holds Master Of Science (M.S.), Pharmaceutical Economics And Policy from University Of Southern California.
Kristina Chen is listed with skills including Health Economics, Data Analysis, Outcomes Research, Clinical Research, Healthcare, Claims Data Analysis, Budget Impact Models, and Analysis.
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