Professional Summary
Seasoned Clinical Research Professional | Global Trial Management | Regulatory Affairs Expertise | Leader in Operational Excellence and Staff Development
Experienced in clinical research coordination & management with a demonstrated history of working in the higher education industry. Strong regulatory professional skilled in Good Clinical Practice (GCP), Healthcare, Leadership, U.S. Food and Drug Administration (FDA) IND & Training the next generation of clinical research professionals.
Publications
Peer Reviewed Publications
Robbie Paulsen MD, Jeffery Hill MD, Erin McDonough MD, Natalie Kreitzer MD, Emily Werff, Brittney Hahn, Sally A. Santen MD, PhD (2024. ) Evaluation of learning in emergency medicine: An umbrella IRB protocol for education outcomes research .AEM Education and Training, , 8 (5 ) ,
Gass A, Eisen H, Griffith B, Kobashigaqa J, Koerner M, Mancini D, Mehra M, Meiser B, Webber S. Young, J, Gilb E, Tuteja S (2001. ) Current practices: immunosuppression induction, maintenance and rejection regimens in 213 consecutive transplant recipients .Journal of Heart & Lung Transplantation , ,
Other Publications
Linke M, McMullan J, Werff E (2018. ) Study Looks at Use of Emergency Research Informed Consent .IRB Advisor – AHC Media,
Presentations
Invited Presentations
Linke M, McMullan J, Werff E. (2017. ) FDA and IRB approval of a novel prehospital consent process for emergency research .PRIM&R 2017 Advancing Ethical Research Conference, San Antonio.
Trisha Wise-Draper, MD, PhD; Justin Osborne; Benjamin Quast, MBA, CCRP; Emily Werff: Michael Hurley, MBA (2018. ) First Place Abstract Presentation .Association of American Cancer Institute’s Clinical Research Initiative Meeting, Chicago, IL.