CV / English / Clinical Program Manager
Victoria R. Lawson
- Email: [email protected]
- Phone: (555) 123-4567
- Address: 987 Healthway Drive, Medical City, FL 33602
Executive Summary
Dynamic and results-oriented Clinical Program Manager with over 8 years of successful experience in leading clinical trials and research projects within cancer treatment and cardiology disciplines. Demonstrated track record in managing cross-functional teams, implementing innovative clinical strategies, and enhancing operational efficiencies. Known for impeccable organizational skills, keen attention to detail, and a compassionate approach to patient care. Seeking to leverage extensive background in clinical program management to drive successful outcomes and advancements in medical research.
Core Competencies
- Clinical Trial Management
- Research Project Leadership
- Regulatory Compliance
- Cross-functional Team Leadership
- Budget Management and Cost Control
- Strategic Planning and Execution
- Patient Recruitment and Retention Strategies
- Data Analysis and Reporting
Technologies and Certifications
- Proficient in Clinical Trial Management Systems (CTMS)
- Experienced with EDC Systems
- Advanced user of Microsoft Office Suite (Word, Excel, PowerPoint)
- Certified Clinical Research Coordinator (CCRC)
- Project Management Professional (PMP) Certification
Professional Experience
Senior Clinical Program Manager ABC Pharmaceuticals, Medical City, FL January 2017 – Present
- Spearheaded multiple phase III clinical trials in oncology, resulting in successful data for new drug applications.
- Led a team of 20+ clinical research associates and data coordinators, ensuring compliance with FDA regulations and protocol adherence.
- Managed project budgets exceeding $5M, optimizing resources and reducing costs by 15%.
Clinical Project Coordinator XYZ Biotech, Tampa, FL June 2015 – December 2016
- Coordinated operations for phase I and II clinical trials in cardiology, achieving 100% compliance with study protocols.
- Implemented patient recruitment strategies that increased enrollment by 25%.
- Facilitated cross-departmental communication to ensure project milestones were met on time.
Clinical Research Associate Clinical Solutions, Orlando, FL March 2012 – May 2015
- Monitored trial sites for adherence to protocol and GCP standards.
- Assisted with the development of study documents, including protocols, informed consent forms, and case report forms.
- Conducted site visits and audits, preparing detailed reports on findings.
Education and Training
M.S. in Clinical Research Administration University of Florida, Gainesville, FL Graduated: May 2014
B.S. in Biology University of Miami, Coral Gables, FL Graduated: May 2011
Professional Development Workshops - Effective Leadership for Managers - Advanced Data Analysis in Clinical Research
Referees
Dr. Emily White Director of Clinical Research ABC Pharmaceuticals Email: [email protected] Phone: (555) 678-9012
Marcus Johnson, PMP Project Manager XYZ Biotech Email: [email protected] Phone: (555) 234-5678