Free Clinical Research Coordinator Resume

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Professional Summary
Dedicated and detail-oriented Clinical Research Coordinator with over 5 years of experience in managing clinical trials and research projects. Expertise in regulatory compliance, patient recruitment, and data management. Proven track record of successful project execution and cross-functional collaboration across all phases of clinical research.
Core Competencies
Clinical Trial Management
Regulatory Compliance
Patient Recruitment and Retention
Data Collection and Management
Protocol Development
Team Leadership and Collaboration
Professional Experience
Clinical Research Coordinator
MedCore Clinical Research Institute, City, State
January 2059 – Present
Coordinate and manage daily operations of clinical trials ensuring adherence to protocol and regulatory requirements.
Recruit, screen, and enroll study participants while maintaining compliance with ethical standards and informed consent processes.
Collaborate with principal investigators and clinical teams to ensure seamless study execution and data integrity.
Monitor and report adverse events and other relevant safety information by FDA and IRB guidelines.
Oversee CRF completion, data entry, and query resolution to maintain the accuracy of data collection.
Assistant Clinical Research Coordinator
Bright Horizons Medical Center, City, State
March 2056 – December 2058
Assisted in the management and coordination of multiple clinical studies from start-up to closure.
Supported the development of study protocols, informed consent forms, and other essential documents.
Facilitated participant recruitment through community engagement and educational events.
Maintained meticulous study documentation and regulatory binders in compliance with GCP standards.
Trained and supervised new research staff in clinical procedures and protocol adherence.
Education
Bachelor of Science in Biology
Greenwood University, City, State
Graduated: May 2055
Certifications
Certified Clinical Research Coordinator (CCRC), ACRP
Good Clinical Practice (GCP) Certification
Technical Skills
Proficient in MS Office Suite and clinical trial management systems (CTMS)
Experience with electronic data capture systems (EDC) such as REDCap and Medidata Rave
Professional Affiliations
Member, Association of Clinical Research Professionals (ACRP)
Member, Society of Clinical Research Associates (SOCRA)
References
Available upon request.
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The Clinical Research Coordinator Resume Template on Template.net is an excellent choice for professionals managing clinical trials. This editable and customizable template allows you to emphasize your organizational skills, regulatory knowledge, and clinical trial management experience. Editable in our Ai Editor Tool, it’s easy to personalize your resume, giving you full control over your document’s content and layout.
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