Brenda J

Brenda J. has a wide range of experience in the clinical research field. Brenda started their career as a Patient Service Representative at Medtronic in 2006, providing phone coverage for patients and developing knowledge of various medical devices. From 2008 to 2010, they worked as a Clinical Studies Support Coordinator (CRA) at Medtronic. In this role, they supported clinical studies and assisted in patient recruitment and screening.

In 2010, Brenda joined Fairview Physician Associates as a Research Study Coordinator. Here, they directly interacted with patients, provided consultation and education to staff, and ensured that clinical trials were conducted according to protocol.

Brenda then moved to Quintiles in 2012, working as a Clinical Research Associate. In this role, they served as the primary communication representative between investigative site and sponsor teams, ensuring compliance with regulations and protocol. Brenda joined Medtronic as a Clinical Research Specialist (CRA) in 2013, where they managed study sites and facilitated communication between study teams and site coordinators.

From 2014 to 2018, Brenda worked at Abbott as a Clinical Research Associate. Here, they independently planned and conducted clinical trials, ensuring compliance with regulatory standards and protocols.

Most recently, Brenda worked at Urotronic, Inc. as a Clinical Manager, starting in 2018. In this position, they developed clinical documents, managed projects, and oversaw clinical trials.

Brenda J. has a Master of Science degree in Regulatory Science from the University of St. Thomas. Brenda also holds a Bachelor of Arts degree in Business Management from Bethel University. Additionally, Brenda J. has an Associate of Applied Science degree in Medical Assistant from the Minnesota School of Business. In April 2016, they obtained the certification of Certified Clinical Research Professional from the Society of Clinical Research Associates (SOCRA).