Sandra Sinclair

Bio:

With over two decades of Clinical Research Operations experience and a background in medicine as a Registered Nurse Sandra has witnessed many Best Practices obtained from working relationships, networking and personal experience from failures and successes throughout her career. She works in Clinical Trial development and participates as a strategy contributor. She facilitates oversight of monitoring, supports regulatory submissions, Data Management and Quality Control Measures. She has overall experience in creating, organizing, and conducting training programs and has focused on education to change behaviors. She supports professional development of teams using a cross functional approach and is a strong supporter of lean processes that meet regulatory compliance. With working knowledge of the Lean Six Sigma concepts for process improvement and streamlining procedures she uses her Leadership, Management, and Supervisory experience to build training materials, policies and procedures (SOPs) and ensures program development includes performance analysis for continuous process improvement.