Expert Details

Pharmaceuticals and Biotechnology

ID: 733745 Ohio, USA

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Expert is a clinical psychologist by training with over 9 years of experience in Health Economics and Outcomes Research. His area of focus is Clinical Outcomes Assessment, including Patient Reported Outcomes. Expert helps sponsors define and implement a COA strategy in their clinical programs leading to actionable patient-centric data which can be included in regulatory submissions and interactions with payers in the US and Europe.

Education

Year Degree Subject Institution
Year: 2004 Degree: PhD Subject: Clinical Psychology Institution: Fordham University
Year: 1997 Degree: MA Subject: Clinical Psychology Institution: Fordham University
Year: 1995 Degree: BA Subject: Psychology Institution: Yeshiva University

Work History

Years Employer Title Department
Years: 2017 to Present Employer: Undisclosed Title: Program Manager, Patient Reported Outcomes Department: Value Evidence and Outcomes
Responsibilities:
• Direct development and implementation of PRO strategies, primarily in the areas of respiratory illness and infectious disease
• Oversee the work of contracted vendors, including scope of work development, contract initiation, and project milestones, timelines, deliverables, and budgets
• Contribute to the design, implementation, and management of registration clinical trials containing PROs; development of the PRO sections of study protocols, statistical analysis plans, clinical study reports and other development documents
• Scientific writing, including regulatory and payer communications and engagement of health care providers as external experts
Years Employer Title Department
Years: 2015 to 2016 Employer: Roche/Genentech Title: Outcomes Research Scientist Department: Patient Centered Outcomes Research
Responsibilities:
• Lead PRO implementation activities for oncology molecules and develop global PRO strategies in breast, lung, and colorectal cancer
• Work cross-functionally with Global Development, Global Product Strategy, International Business Teams, Global Health Economics and Affiliates to direct the implementation of PRO strategies
• Contribute to the design, implementation, and management of registration clinical trials containing PROs; development of the PRO sections of study protocols, statistical analysis plans, clinical study reports and other development documents
• Scientific writing, including regulatory and payer communications and stakeholder engagement
Years Employer Title Department
Years: 2013 to 2015 Employer: Truven Health/Watson IBM Title: Senior Research Leader Department: Strategic Consulting
Responsibilities:
• Directed all PRO activities within HEOR consulting group, including business development
• Collaborated on claims, EHR, RWE, and dossier projects
• Worked across therapeutic areas/indications including oncology, CNS, GI, GU, musculoskeletal, pediatric

Fields of Expertise

biomedical research and development, pharmacoeconomics, drug development, biopharmaceutical product development, biopharmaceutical

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