Dawn Serkin, RN, BScN

Dawn Serkin, RN, BScN has over 13 years of experience in clinical trial management and clinical operations in the pharmaceutical industry. From 2007 to 2013, they worked as a Senior Clinical Research Associate at ClinSmart LLC where they were responsible for the development of study documentation such as protocols, informed consents, case report forms, validation rules and final study reports. From 2013 to 2015, they worked as a Clinical Trial Site Management | Senior CRA at Novo Nordisk Inc. where they were responsible for the support of assigned studies in accordance with Good Clinical Practice (GCP), ICH guidelines and federal regulations. From 2015 to 2018, they worked as a Clinical Site Management | Site Lead in the pharmaceutical industry as an independent contractor, where they were accountable for the oversight and management of clinical trial activities at the investigator site. In 2018, they began working at ClinSmart as a Clinical Trial Management | Clinical Operations, where they were responsible for the overall operational planning and activities for the implementation and conduct of clinical trials in compliance with ICH, GCP’s, SOPs, and local requirements.

Dawn Serkin, RN, BScN obtained their Bachelor of Science in Nursing (BScN) from Gwynedd Mercy University with a focus on Research Nurse and Clinical Nursing. Dawn holds additional certifications, including CRA Certification from Barnett International, Certification in Oncology from Fox Chase Cancer Center, Certified in Nursing Management from University of Pennsylvania, Clinical Research Coordinator Certification from Jefferson Health - Northeast, Human Subjects Protection Certification from CITI Program, A Division of BRANY, and Informed Consent and Assent from Firecrest Clinical.