Rosemary Zang joined SPR Therapeutics as a Senior Clinical Project Manager. Prior to joining SPR, Ms. Zang spent over 4 years in her role as a Sr. Clinical Project Manager at
NDI Medical, the parent company of SPR, where she oversaw clinical study activities, monitored studies for compliance with Good Clinical Practices, and contributed to various FDA regulatory submissions.
Ms. Zang has held various positions throughout her 20+ years in the medical device industry. Prior to joining NDI Medical, she oversaw orthopaedic clinical study activities for several large scale multi-center clinical studies. She has worked on PMA applications, 510(k) submissions and re-classification petitions. Ms. Zang also designed, implemented and monitored post market clinical trials for commercially available orthopaedic products. In addition to her industry experience, Ms. Zang also had her own independent consulting business which provided clinical research support services to device organizations that promoted improved GCP compliance, productivity, and safety. Before joining the medical device industry she developed a strong clinical background by planning and administering high-tech care to critically ill medical and surgical patients as a critical care nurse.