CERobs Consulting LLC
Cynthia Girman has a diverse work experience in various fields. Cynthia is currently working as a Book Author at Wings of Peace Press, LLC, where they authored a book called "A Voice from Heaven: From Earthly Struggles to Thriving in the Afterlife" that was released in May 2023. Prior to this, Cynthia founded and served as the President of CERobs Consulting LLC since 2015, providing consulting services on various research methodologies and protocols. Cynthia also served on the Methodology Committee and Clinical Trials Advisory Panel at the Patient-Centered Outcomes Research Institute (PCORI) in 2014. Cynthia has also worked as an Adjunct Professor at UNC Gillings School of Global Public Health since 2006. Cynthia began their career in 1981 at Merck Research Laboratories, where they held the position of Executive Director and led various research and analytics teams.
Cynthia Girman received their Bachelor of Science in Public Health (BSPH) with a focus on Biostatistics from the University of North Carolina at Chapel Hill in 1981. Cynthia then pursued a Master of Science (MS) in Applied Statistics and Computer Science from Villanova University, completing it in 1986. In 1994, Cynthia obtained their Doctorate of Public Health (DrPH) with a specialization in Biostatistics and Epidemiology from the University of North Carolina at Chapel Hill.
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CERobs Consulting LLC
CERobs Consulting, LLC provides individualized consulting services for study design, methods and improvement of patient-centered outcomes research, comparative effectiveness research, pragmatic randomized trials and real world evidence observational research. Consulting services range from conceptualization of research questions and endpoints to protocol development and manuscript preparation. CERobs offers services & consulting in: 1. Observational studies and registries 2. Comparative effectiveness research (CER) 3. Pragmatic randomized trials (pRCTs) 4. Randomized controlled clinical trials 5. Data science in real world evidence (RWE) 6. Post-Authorization Safety Studies (PASS) 7. Patient engagement and patient experience data 8. Clinical outcome assessment (development & validation) 9. Systematic literature reviews and meta-analyses