Free Clinical Research Coordinator Resume Template
Clinical Research Coordinator Resume
Address: [Your Address]
Phone: [Your Phone Number]
Email: [Your Email]
LinkedIn: https://www.linkedin.com/in/your_own_profile
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
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Clinical Trial Management
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Regulatory Compliance
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Patient Recruitment and Retention
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Data Collection and Management
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Protocol Development
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Team Leadership and Collaboration
Professional Experience
Clinical Research Coordinator
MedCore Clinical Research Institute, City, State
January 2059 – Present
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Coordinate and manage daily operations of clinical trials ensuring adherence to protocol and regulatory requirements.
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Recruit, screen, and enroll study participants while maintaining compliance with ethical standards and informed consent processes.
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Collaborate with principal investigators and clinical teams to ensure seamless study execution and data integrity.
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Monitor and report adverse events and other relevant safety information by FDA and IRB guidelines.
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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
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Assisted in the management and coordination of multiple clinical studies from start-up to closure.
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Supported the development of study protocols, informed consent forms, and other essential documents.
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Facilitated participant recruitment through community engagement and educational events.
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Maintained meticulous study documentation and regulatory binders in compliance with GCP standards.
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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
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Certified Clinical Research Coordinator (CCRC), ACRP
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Good Clinical Practice (GCP) Certification
Technical Skills
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Proficient in MS Office Suite and clinical trial management systems (CTMS)
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Experience with electronic data capture systems (EDC) such as REDCap and Medidata Rave
Professional Affiliations
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Member, Association of Clinical Research Professionals (ACRP)
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Member, Society of Clinical Research Associates (SOCRA)
References
Available upon request.
