Nela Hayes is a seasoned professional with over 18 years of experience in the biopharmaceutical industry. Known for her collaborative and problem-solving skills, she excels as a strategic leader who emphasizes cross-functional harmonization and operational excellence. With a Bachelor's degree in Communication Studies from Northwestern University, Nela has a strong foundation in communication and leadership.

Throughout her career, Nela has held various key roles at reputable organizations such as Novartis and AbbVie. Her expertise includes building teams, global clinical trials management, vendor management, site and sponsor inspections, NDA/MAA submissions, clinical documentation management, ICH/GCP regulations, and process improvement. She has a proven track record in leading cross-functional teams and ensuring compliance with regulatory standards.

At Novartis, Nela served as the Head of Clinical Document Management Process and previously held positions as TMF Governance Lead and Director of Clinical Documentation & Process Excellence. Prior to her time at Novartis, she garnered experience at AbbVie and Abbott in roles ranging from Clinical Research Associate to Documentation Specialist/Change Request Coordinator. Nela's diverse background reflects her adaptability and expertise in various aspects of clinical research and documentation.

Nela Hayes is a dedicated professional passionate about helping individuals and teams achieve their full potential. Her focus on empathy, adaptability, and operational excellence sets her apart as a leader committed to driving success in the biopharmaceutical industry.