Experience

Regeneron

• United States
• Biotechnology
• 700 & Above Employee

• Senior Manager- Global Trial Optimization

  • Sep 2022 - Present



Boehringer Ingelheim

• Germany
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Feasibility Manager

  • Mar 2019 - Sep 2022



Parexel

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Feasibility & Strategy Lead

  • Jul 2017 - Feb 2019



Boehringer Ingelheim

• Germany
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Feasibility and Site Identification

  • May 2016 - Jul 2017

  • Develop and maintain relationships with investigators, study coordinators, other site personnel, and members of other ClinOps departments. • Seeks to understand and uphold trial site selection strategies, inclusive of trial timelines • Tracks and maintains metrics of daily investigator/site contact activities (ex. vetting requests, eSurveys, investigator follow-up by phone/email, etc.) • Develops pools of potential investigators from a variety of internal and external sources based… Show more • Develop and maintain relationships with investigators, study coordinators, other site personnel, and members of other ClinOps departments. • Seeks to understand and uphold trial site selection strategies, inclusive of trial timelines • Tracks and maintains metrics of daily investigator/site contact activities (ex. vetting requests, eSurveys, investigator follow-up by phone/email, etc.) • Develops pools of potential investigators from a variety of internal and external sources based on trial specific investigator profiles • Assesses initial interest of overall pool for basic site capabilities, investigator qualifications and access to patient population. • Designs study specific questionnaires for the assessment of country specific feasibility information including but not limited to protocol design, investigator type, site and trial capabilities, patient population, etc. • Develops and maintains feasibility metrics and status reports (ex. process cycle time, quality of recommendations, issues/risk mitigation, etc.) to support data-driven decisions Show less



Medpace

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Feasibility Associate

  • Dec 2013 - May 2016

  Cincinnati, Ohio Area • Evaluate and support new clinical trial opportunities by working with Medical Experts, Clinical Trial Managers and our Regulatory Submissions team • Collaborate with international country managers and external resources to develop feasibility strategies across multiple therapeutic areas • Assess the Competitive Landscape and Epidemiology of a drug and/or indication to identify the most efficient way to conduct a trial. • Manage start-up activities for all paid feasibility… Show more • Evaluate and support new clinical trial opportunities by working with Medical Experts, Clinical Trial Managers and our Regulatory Submissions team • Collaborate with international country managers and external resources to develop feasibility strategies across multiple therapeutic areas • Assess the Competitive Landscape and Epidemiology of a drug and/or indication to identify the most efficient way to conduct a trial. • Manage start-up activities for all paid feasibility projects, including feasibility questionnaire analysis, site identification, and site selection • Develop text and slides for proposals and bid defenses in coordination with the proposal writers and business development executives. Show less



INC Research

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Global Feasibility Analyst

  • Jun 2012 - Nov 2013

  Cincinnati, Ohio Area •Conduct analysis of internal, external, site level and therapeutic data to determine optimal distributions for clinical trials in response to proposals and stand-alone feasibility projects. Present information via proposal text and in person client meetings including bid defenses. •Assess aspects of protocol and develop operational strategies including scenario planning country and site level optimization, tailoring analysis to address client needs and utilize predictive investigator… Show more •Conduct analysis of internal, external, site level and therapeutic data to determine optimal distributions for clinical trials in response to proposals and stand-alone feasibility projects. Present information via proposal text and in person client meetings including bid defenses. •Assess aspects of protocol and develop operational strategies including scenario planning country and site level optimization, tailoring analysis to address client needs and utilize predictive investigator performance metrics to facilitate forecasting. •Work closely with an international project management, medical and business development/proposal members to deliver robust feasibilities to clients within defined scope and timelines. Show less



TriHealth

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Research Specialist

  • Dec 2009 - Jul 2012

  • Assist Obstetrics and Gynecology residents and physicians with their research design and study proposal. • Complete all IRB regulatory documents for the TriHealth Ob-Gyn department • Perform statistical analysis on research studies completed by TriHealth Ob-Gyn residents. • Aid in the writing of manuscripts for publication and creation of posters for national meetings.



University of Cincinnati

• United States
• Higher Education
• 700 & Above Employee

• Ohio River Valley Study Coordinator

  • Jul 2009 - Dec 2009

  Assisted in the organization of data collection trips and coordinated data entry. Formulated interview questionnaire questions and administered the interview questionnaires to study participants. Assisted in reporting data results to study participants.