Prior to joining COS, Jessica worked as a Legal Assistant before transitioning to the field of clinical research. She worked for a company that provides photography services for clinical trials. She has worked on various photographic aspects of clinical trials – including processing and QC of clinical images. Within this company she also provided GCP, Quality Assurance, and Regulatory Support.

Jessica’s Quality Assurance background includes: Privacy of Protected Health Information; Regulatory (FDA) Guidelines; GCP quality system development and compliance – including overall study-specific compliance; study documentation standards for various clinical trial phases; creation and review of Standard Operating Procedures (SOPs); creation and maintenance of standardized forms and templates; managing study-specific procedural documents; providing support for various types of audits related to photographic study documentation; and ensuring clinical photography is in alignment with industry standards.

Jessica comes to COS from New Jersey by way of California. She is highly experienced in the fast-paced culture of clinical trial support and committed to success. With a natural penchant for detail and organization, she remains strong in her east coast roots while enjoying a west coast way of life.

She holds a Bachelor’s Degree in English Literature with a minor in Writing from William Paterson University, Wayne, New Jersey.