Founder & CEO

• May 2019 - Present

Bridging research and community health Bridging research and community health

Member Board of Trustees

• Mar 2023 - Present

The Trenton Community Improvement Corporation (CIC) supports economic and community development activities. The CIC is authorized by Section 1724.10 of the Ohio Revised Code and Chapter 236 of the City Code. The CIC’s duties and powers include: A non-profit instrument for the City to facilitate industrial, commercial, distribution and research development; Create opportunities for employment; Increase tax valuation; and Sell and buy property. The Trenton Community Improvement Corporation (CIC) supports economic and community development activities. The CIC is authorized by Section 1724.10 of the Ohio Revised Code and Chapter 236 of the City Code. The CIC’s duties and powers include: A non-profit instrument for the City to facilitate industrial, commercial, distribution and research development; Create opportunities for employment; Increase tax valuation; and Sell and buy property.

Member Board of Trustees

• Mar 2023 - Present

Member Of The Board Of Advisors

• Aug 2020 - Present

The mission of the Wittenberg Institute for Public Humanities and Sciences is: 1. To provide learning and research opportunities for students in public-facing humanities and sciences through curricular and co-curricular opportunities and faculty-student collaborations. 2. To increase the amount and range of faculty teaching, projects, and research in public-facing humanities and sciences. 3. To train, support, and further the work of faculty who are engaging in public facing work. 4. To create a regionally and nationally connected institute to foster the growth of public-facing humanities and sciences through innovative inter-institutional collaborations. These will include collaborations with ELCA institutions, SOCHE institutions, and Research 1 institutions. 5. To create a culture at Wittenberg and beyond our campus where the utilization of the humanities and sciences for the public good is recognized and valued. 6. To initiate a new signature program every two years that is responsive to the needs or trends of the public, which can be engaged through work in the humanities and sciences. Show less

Board Member

• Feb 2022 - Nov 2022

Board Member

• 2016 - Oct 2022

The Conscious Connect Community Development Corporation (CDC) is committed to advancing equitable park and green space access for all residents in Southwest Springfield. We are looking for individuals to join our People, Parks, and Power (P3) team that are community-driven, motivated learners, and committed to social justice. The Conscious Connect Community Development Corporation (CDC) is committed to advancing equitable park and green space access for all residents in Southwest Springfield. We are looking for individuals to join our People, Parks, and Power (P3) team that are community-driven, motivated learners, and committed to social justice.

Advisory Board Member

• Oct 2021 - Jun 2022

Feasibility Analyst

• 2019 - 2020

• Oversee the site information collection process and assess compiled information for trends and site capabilities. • Conducted independent standalone site outreach projects as needed • Present and explain feasibility analysis to BD/Clients • Assist with the development, expansion, and maintenance of resource library of therapeutically alignment materials for organizational reference and educational purpose • Collects and analyzes metric-based global intelligence for pre-award strategic clinical trial development Show less

Global Marketing Feasibility Analyst

• Aug 2018 - 2019

• Oversee country, therapeutic, marketing landscape assessments (standard of care, media channels and utilization, country attitudes toward clinical trials, language/country nuances, prevalence/incidence) • Develop an analysis from all data insights to formulate market feasibility recommendations; The report includes, but not limited to, general disease state information, an updated list of countries based on prevalence/incidence, updated list of country/therapeutic challenges, competitive studies, media restrictions, advocacy partnerships, Physician type/role in decision making, strategic and operational challenges to execute the protocol • Lead the development of the marketing feasibility plan through assessing the needs of the project and specific studies to define the end-to-end feasibility approach. • Provide insights on challenges and opportunities as well as a set of recommendations to inform the recruitment strategy • Liaison with Site Network to validate country knowledge and trends, insure country requirements are captured and integrated • Exploring new opportunities to add value to the organization and departmental processes Show less

Feasibility Coordinator

• Jan 2018 - Jul 2018

• Support feasibility assessments by reviewing study protocols/documents and collecting and collating internal and external data and information • Contribute to writing feasibility sections of proposals • Collaborate with Medical Directors, Clinical Trial Managers and Principal Investigators to help determine the feasibility of clinical trials • Support feasibility assessments by reviewing study protocols/documents and collecting and collating internal and external data and information • Contribute to writing feasibility sections of proposals • Collaborate with Medical Directors, Clinical Trial Managers and Principal Investigators to help determine the feasibility of clinical trials

Senior Research Associate (performed feasibility duties as well)

• Jun 2017 - Dec 2017

• Tracked patient visits, assured completion of electronic case report forms, and organized and reported meeting minutes• Reconciled the trial master file and filed appropriate documents• Performed advanced internet searches and summarized articles on company and product information• Trained and mentored new Research Associates• Evaluated Citeline™ software for utilization by business development

Research Associate

• Apr 2016 - Jun 2017

• Organized, composed, and produced professional letters, summaries, reports, and minutes using Microsoft Office applications, including Word, Access, and Excel• Assembled a Microsoft Excel database and converted it to Microsoft Access comprising >10,000 potential investigators for clinical trials using the internet through clinicaltrials.gov• Developed proficiency in using Microsoft Office applications, including Word, Access, Powerpoint, and Excel• Created professional binders for distribution to clients Show less

Clinical Research Assistant

• Nov 2015 - Mar 2016

• Participated in screening subjects for a clinical trial in immunology • Extracted pollen samples during specified intervals according to the study protocol within the Environmental Exposure Chamber (EEC), including staining and counting pollen grains using a compound microscope • Monitored subjects during in-house confinement periods for protocol and Standard Operating Procedures (SOP) requirement, such as physical restrictions, water restrictions, meals, and fluid intake and output • Calibrated and maintained EEC per SOPs and maintained appropriate logbooks • Prepared and reviewed study related materials, such as study tube labels and clipboard preparation, for completeness and accuracy while assuring the clinic was prepared with required supplies • Utilized and tracked clinical trial patient visits and information through the Clinical Trial Management System Show less

Global Site Identification Specialist

• Sep 2014 - Nov 2015

• Worked as Lead Site Identification Specialist on three separate global projects • Performed as project lead in site feasibility ascertainment with pharmaceutical clients to recruit sites for clinical studies • Assured agreement between budgetary estimates and site recruitment needs on a global basis • Worked to identify client needs to recruit investigators with sufficient patient population for new product development • Fostered communication between investigator sites and sponsors in order to coordinate and update Confidentiality Disclosure Agreements and FDA regulatory documents and reports • Provided weekly update reports to pharmaceutical companies on budgeting needs, efficiencies, and hours of staff • Tracked submissions and ensured timely filing of documents Show less