Sandra Johnson

Sandra Johnson is a seasoned clinical research professional with extensive experience in study start-up and clinical operations. Currently serving as Senior Country Study Start-Up Specialist at AbbVie, she brings over a decade of expertise in managing clinical trials, regulatory submissions, and cross-functional team coordination. Her career is marked by a strong track record of successfully initiating and executing complex studies across multiple therapeutic areas, ensuring compliance with global regulatory standards and timelines.

Sandra began her career supporting legal and administrative functions for prominent law firms and pharmaceutical organizations, developing a foundation in contract negotiation, document management, and executive-level support. Over the years, she transitioned into clinical research, holding key roles at PRA Health Sciences, inVentiv Health Clinical, and Allergan, where she gained hands-on experience in study start-up management, site feasibility, contract execution, and clinical trial coordination. Her ability to navigate complex processes and mentor team members has been central to her professional growth and the successful outcomes of the studies she oversees.

A graduate of Aspen University with a Bachelor of Science in Business Administration, Sandra combines her business acumen with clinical expertise to drive operational excellence in clinical research. She is recognized for her attention to detail, strategic problem-solving, and dedication to advancing healthcare through meticulous study execution. Beyond her professional achievements, Sandra actively advocates for workforce equity and mentorship, inspiring colleagues and the broader industry through her leadership and commitment to inclusive growth.

• Aspen University

• Food Bank