Pilar Waling-May

About Pilar Waling-May

With over 20 years of experience in the Drug Development and Clinical Trials industry, I have built a career within the CRO environment, progressing through roles such as Project Associate, Clinical Regulatory Specialist, Clinical Research Associate (Levels Clinical Team Manager, Country Study Start-Up Lead, and Manager of Clinical Operations.I am passionate about advancing clinical research and contributing to studies that improve patient outcomes and shape the future of medicine. I thrive in environments where curiosity, precision, and collaboration drive meaningful discoveries. My mission is to support high-quality clinical trials by ensuring regulatory compliance, maintaining data integrity, and upholding the highest ethical standards. I’m motivated by the opportunity to bridge science and patient care—turning research into real-world impact.Core Strengths & Specialties-Analytical and administrative proficiency-Cross-functional collaboration-Risk mitigation and problem-solving-Process development and implementation-Project resourcing and team coordination-Training, mentoring, and people management-Performance management and stakeholder engagement-Exceptional communication and interpersonal skills-Technology proficiency and data integrity assurance

Experience

1. Manager of Clinical Operations

   ICON plc

   Jul 2021 — Present · Wilmington, NC, US

Education

• University of North Carolina at Wilmington

  Bachelor of Science

Skills

• Regulatory Submissions
• CRO
• Clinical Data Management
• Sop
• Gcp
• Clinical Research
• Edc
• Therapeutic Areas
• Ctms
• Infectious Diseases
• Clinical Development
• Clinical Trials
• Oncology
• Ich-Gcp
• Clinical Monitoring