Connie Ross

Connie Ross has a diverse work experience spanning over several years. Connie started their career as a Sales Associate at Ann Taylor Retail, where they excelled in retail sales and customer service. Connie then transitioned to working as a Leasing Consultant and Social Director at Towne Properties, where they leased apartment homes and organized social activities.

In 2008, Connie entered the field of clinical research. Connie first worked as a Clinical Research Associate at Medpace, where they conducted pre-study, initiation, monitoring, and closeout visits, ensuring adherence to SOPs and guidelines. Connie then became a Clinical Research Coordinator at Sleepcare Diagnostics, Inc., where they focused on medical device studies related to sleep disorders.

Connie's career in clinical research continued with roles at Camargo Pharmaceutical Services and Advarra. At Camargo, they served as a Clinical Research Associate and Medical Writer, helping to facilitate projects in clinical operations and writing/revising protocols and study documents. At Advarra, Connie was an Affiliated Board Member II, specializing in regulatory and human subject research protection.

In recent years, Connie has held positions as an IRB Program Manager at Lukos, Bestica Inc., and SIERTEK LTD. Connie'sresponsibilities in this role involve overseeing institutional review boards and managing the program.

Overall, Connie Ross has built a strong background in clinical research, regulatory compliance, and customer service throughout their career.

Connie Ross earned a Bachelor of Science degree with High Distinction in Pre-Medical Sciences from Eastern Kentucky University, where they studied from 1976 to 1981. Connie then continued their education at the Medical College of Ohio at Toledo from 1981 to 1983, focusing on Medicine.