On-Site Clinical Research Coordinator Resume
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Phone: [Your Phone Number]
Email: [Your Email]
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Objective
To secure an On-Site Clinical Research Coordinator position where I can utilize my expertise in managing clinical trials, ensuring protocol compliance, and handling patient recruitment to contribute to cutting-edge research and improve patient outcomes.
Education
Master of Science in Clinical Research
University of Science, Cityville, State | Graduated: May 2052
Bachelor of Science in Biology
State University, Townville, State | Graduated: May 2050
Professional Experience
Clinical Research Coordinator
Health Research Institute, Cityville, State | June 2054 - Present
Coordinate and oversee clinical trials, ensuring compliance with federal regulations and protocol guidelines.
Manage patient recruitment, enrollment, and follow-up activities, maintaining high retention rates.
Develop and update essential study documents, including informed consent forms and case report forms.
Collaborate with principal investigators and sponsors to ensure timely completion of study milestones.
Clinical Research Assistant
Medical Center, Townville, State | June 2052 - May 2054
Assisted in the organization and coordination of clinical trials with a focus on patient safety and data integrity.
Collected, processed, and analyzed research data, ensuring accuracy and confidentiality.
Supported the clinical team in daily operations, including scheduling participant visits and handling patient inquiries.
Certifications
Certified Clinical Research Coordinator (CCRC)
Skills
In-depth knowledge of FDA regulations and GCP guidelines
Excellent patient communication and interpersonal skills
Proficient in electronic data capture systems (EDC)
Strong organizational and problem-solving abilities
Professional Affiliations
References
Available upon request.
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