Robin is a highly accomplished and top-performing clinical operations expert with nearly 30 years of success in leading all aspects of clinical operations, including outsourcing management, risk mitigation, budget/resource management, process/system improvement, and strategic planning. She excels in managing Phase 1-4 clinical research programs and has expertise in CNS, diabetes, gastroenterology, oncology, women’s health, inflammation/pain, cardiovascular disease, ophthalmology, autoimmune conditions,…
Kelli’s career in the pharmaceutical industry started in 1998 at Parke Davis as a data manager. Over the years she has worked at various pharma and biotech companies both large and small, on the CRO side as well as the sponsor side. Other experience includes clinical study operations manager and CRA roles. Most recently, Kelli has started consulting with Blue…
Diana is a seasoned professional in Clinical Research with over 25 years of experience in both monitoring and clinical operations. Her expertise in ICH and GCP guidelines, combined with her experience in Clinical Monitoring, makes her highly skilled in both Monitoring and Vendor Oversight. She is also proficient and knowledgeable in Trial Master File management. Her expertise and leadership extend…
Amy’s career in the industry began at Parke-Davis / Pfizer in the 1990s, where she quickly made her mark, diving into countless protocols across a range of roles. Her journey has been anything but ordinary—she’s stepped up to tackle everything from FDA Sponsor Audits to rescuing Trial Master Files and untangling complex clinical trial data. Outside of work, Amy is…