CV / English / Research Study Coordinator

Personal Information

Address: 475 Oakwood Avenue, Pleasantville, NJ, 05888 Email: [email protected] Phone: +1 (555) 876-5432

Brief

A detail-oriented and highly organized Research Study Coordinator with over 5 years of experience in managing and coordinating various research projects within the healthcare sector. Proficient in ensuring studies are conducted in accordance with research protocols, standard operating procedures, and regulatory requirements. Demonstrates a strong ability to collaborate with research teams, manage participant recruitment, and ensure data integrity and confidentiality. Adept at navigating complex research environments and contributing to the successful completion and documentation of research studies.

Core Competencies

• Research Project Management
• Regulatory Compliance & Ethics
• Patient Recruitment & Consent
• Data Collection & Management
• Team Collaboration
• Budgeting & Resource Allocation
• Problem-Solving Skills
• Strong Organizational Skills

Technologies and Certifications

• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)
• Experienced in using REDCap for data management
• Familiar with EDC systems (e.g., Oracle Clinical, Medidata Rave)
• Certified Clinical Research Coordinator (CCRC)
• Good Clinical Practice (GCP) Certification
• HIPAA Compliance Training

Professional Experience

Johns Hopkins University, Baltimore, MD

Research Study Coordinator, September 2018 - Present - Coordinated over 20 research studies across various medical fields, ensuring all projects adhered to protocols, regulations, and timelines. - Led patient recruitment efforts, achieving a 95% target enrollment rate across studies. - Managed study budgets, including resource allocation and expense tracking, to stay within funding constraints.

Central Hospital, New York, NY

Research Assistant, June 2016 - August 2018 - Supported principal investigators in the daily management of research studies. - Assisted with patient recruitment, data collection, and the preparation of regulatory documents. - Contributed to the development of study materials and standard operating procedures.

Education and Training

• Master of Science in Public Health, University of California, Berkeley, 2015
• Bachelor of Science in Biology, Rutgers University, New Brunswick, NJ, 2013
• Various professional development workshops on research ethics, data management, and study coordination

Referees

Available upon request.