Lindsey Murray Email and Phone Number
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Experienced Researcher with a demonstrated history of working in the development, evaluation, and qualification of Clinical Outcome Assessment (COA) tools. Skilled in Clinical Trial Analysis, Patient Reported Outcomes, Drug Development, and Clinical Trials. Strong research professional with a Doctor of Philosophy - PhD focused in Epidemiology from The George Washington University- Milken Institute School of Public Health.
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Executive DirectorCritical Path Institute (C-Path) Jan 2022 - PresentProvide scientific and operational leadership for this pre-competitive public-private partnership among C-Path, FDA, the National Organization for Rare Disorders (NORD), other governmental and non-governmental organizations, and key partners in the biopharma, clinical research and patient communities that are seeking and/or developing treatments for rare diseases.
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Associate DirectorCritical Path Institute (C-Path) Sep 2019 - Jan 2022Establish Rare Disease Consortium within the PRO Consortium to support the development of a rare disease COA toolkit.
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Research ScientistEvidera Apr 2017 - Aug 2019Bethesda, Md, Us• Design and conduct health outcomes research funded by pharmaceutical clients. Areas of expertise include clinical outcome assessment (COA) tool development and epidemiology. Research has been in a range of medical areas including pulmonary and respiratory disease, psychiatric illness, pediatric gastroenterology, diabetes, and others. • EXACT PROgram Director. • Provide scientific leadership within project teams independently in the conceptualization and execution of outcomes research studies. -
Senior Research AssociateEvidera Mar 2012 - Apr 2017Bethesda, Md, Us• Scientific responsibilities include directing qualitative and quantitative studies focused on PRO instrument development/validation; supervising data collection; developing statistical analysis plans; developing study protocols; reviewing and synthesizing medical literature; conducting interviews and focus groups; disseminating study results at professional conferences; writing manuscripts for publication in peer-reviewed journals; and written and in-person communication with the FDA and EMA regarding PRO instrument development. • EXACT-PRO Initiative Program Manager • Supervised 4 junior staff members.
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Research Associate IiiUnited Biosource Corporation Aug 2010 - Mar 2012• EXACT-PRO Initiative Program Manager• Scientific responsibilities included preparing, reviewing and editing reports, manuscripts, and poster presentations for submission to professional journals and conferences; Liaised directly with clients regarding data analysis and interpretation, clinical trial endpoints; study design, budgets, proposals; Managed data collection and organization, quality control, developed data entry rules and validation schema, and drafted statistical analysis plans; Finalized protocols, including interview guides for focus group, cognitive debriefing interviews, physician interviews and questionnaire validation studies; Developed search strategies and conducted literature and web searches to retrieve project-related articles and summarized data in literature tables, spreadsheets, and reviews.• Supervised one junior staff member.
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Research Associate IiUnited Biosource Corporation Mar 2008 - Aug 2010• EXACT-PRO Initiative Translation Manager• Scientific responsibilities included drafting study results for scientific dissemination; Liaised directly with clients; Managed data collection and organization, quality control; Developed protocols for focus group, cognitive debriefing interviews, physician interviews and questionnaire validation studies; Managed and executed site recruitment and retention, site budgets, and IRB submissions;• Supervised one junior staff member.
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Research Associate IUnited Biosource Corporation Mar 2007 - Mar 2008• Assisted with design and conducted health outcomes research for public and private clients. Scientific responsibilities included design and implementation of health outcomes studies; instrument development/ validation; developing study protocols, site training materials, data collection procedures, and outcomes instruments; data collection and entry; conducting patient interviews, patient cognitive debriefings, assisting in focus group moderation and conducting clinical expert interviews; investigator/site training; conducting literature reviews; synthesizing medical literature; dissemination; report writing; and preparing manuscripts for publication in peer-reviewed journals.
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Research AssistantUnited Biosource Corporation Aug 2006 - Mar 2007• Responsibilities included literature searching, site management, data collection, data review, IRB submission, proof reading, case report form design, drafting study manuals and library management.
Lindsey Murray Skills
Lindsey Murray Education Details
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The George Washington University- Milken Institute School Of Public HealthEpidemiology -
The George Washington University- Milken Institute School Of Public HealthMaster Of Public Health - Mph
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The George Washington University- Milken Institute School Of Public HealthHealth Promotion
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University Of VirginiaGeneral And Anthropology
Frequently Asked Questions about Lindsey Murray
What company does Lindsey Murray work for?
Lindsey Murray works for Critical Path Institute (C-Path)
What is Lindsey Murray's role at the current company?
Lindsey Murray's current role is Executive Director at Critical Path Institute (C-Path).
What is Lindsey Murray's email address?
Lindsey Murray's email address is li****@****era.com
What schools did Lindsey Murray attend?
Lindsey Murray attended The George Washington University- Milken Institute School Of Public Health, The George Washington University- Milken Institute School Of Public Health, The George Washington University- Milken Institute School Of Public Health, University Of Virginia.
What skills is Lindsey Murray known for?
Lindsey Murray has skills like Qualitative And Quantitative Research Methodologies, Data, Qualitative Research, Clinical Trials, Clinical Trial Analysis, Pharmaceutical Industry, Research, Drug Development, Patient Reported Outcomes, Clinical Outcomes, Science, Statistics.
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