Meredith Calloway Email & Phone Number

Las Vegas, Nv, Us

Arlington, Va, Us

As Director of Evidence Synthesis at the American Diabetes Association, I am proud to conduct scientific research informing the fight against diabetes. My teammates and I are currently working on systematic reviews addressing technology, pharmaceuticals, and nutrition for the treatment of diabetes. Visit diabetes.org to learn more about diabetes, access valuable free resources including Standards of Care and a recipe hub, and how you can take a stand against diabetes.

Houston, Texas, Us

At symplr Content Operations, my goal was to harness the power of clinical evidence, cost analysis, spend analytics, and workflows to provide a powerful suite of tools and services through symplr's Software as a Service platforms. These tools empower payers, providers, and suppliers to make optimal decisions and strategic choices. Responsibilities included integrating acquired companies into "One symplr"; organic growth; provision of effective operational direction; Go To Market; People Management; Support M&A Efforts; New Product Development & Launch; oversight of content development including HTA. People manage team of 55 FTEs including scientists, clinicians, engineers, and managers, plus contractors. Our services use data and resources to inform customers' decisions, including Health Technology Assessment, quotation analysis, and financial guidance.

Houston, Texas, Us

Joined symplr through acquisition. Responsible for direction of HTA preparation, editing, quality assurance; strategic direction; research methodology; product development; topic scoping, selection, and scheduling; analyst training and mentorship; sales and marketing support; profits and losses.

Dallas, Texas, Us

Joined TractManager through acquisition. Preparation of custom/contract reports, Clinical Research Reports, and Evolving Evidence Reviews in a cooperative/cross-functional team environment. Additional responsibilities include product development; management of HTA and brief report preparation and editing; scientific project management; sales and marketing support; operations support.

Preparation of custom/contract reports and proprietary HTAs in a cooperative/cross-functional team environment. Responsible for all aspects of HTA development, and contract management.

Falls Church, Virginia, Us

MANILA Consulting Group (no longer a legal entity) was acquired by Insignia and persisted as a division.Roles included: Clinical Research Project Manager / Deputy Director; Systematic Review Program Manager; Institutional Review Board / Deputy Chair

Plymouth Meeting, Pennsylvania, Us

Roles in evidence-based clinical information development included technical project management, research methodology development, and research analysis-Technical management, research analysis, and preparation of comprehensive systematic quantitative evidence reports in diverse clinical areas. Tasks included protocol development, data extraction, identification of evidence bases, quality assessment, meta-analyses, writing and editing, and technical supervision of research assistants and clinical writers. Prepared several hundred short-turnaround custom reports on medical technology prepared for third party payers and hospital systems.-Training, internal and business-to-business. Led webinar-based client training sessions for evidence use support and presentations to potential clients. Provided training on evidence review for analysts and clinical writers and reviewed other analysts’ quantitative evidence reports and narrative syntheses.

Honors Bachelor Of Science (Bs), With Distinction, Animal Sciences

Master Of Science In Management (Msm), With A Concentration In Health Care Administration

Master Of Science (Ms), Biological Sciences