Expert Details
Pharmaceuticals and Biotechnology
ID: 733745
Ohio, USA
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 |
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| 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 |
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| 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 |
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Government Experience
| Years | Agency | Role | Description |
|---|---|---|---|
| Years: 1998 to 2002 | Agency: US Department of Veterans Affairs | Role: Researcher, Psychology Intern | Description: Research in mental health and substance abuse disorders; training in serious mental illness, neuropsychology, posttraumatic stress, and pain |