Sample CRC Resume

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Sample Clinical Research Coordinator Resume Paul Smith 2365 S Mayfield Ave Chicago, IL 60652 Cell: 123-555-1234 email: paul@anymail.com Summary of Objective: Seeking a challenging and responsible position as a clinical research coordinator, where I can contribute my knowledge and experience in a health care organization. Summary of Skills:       

In-depth knowledge of the methods and principles of clinical practices Extensive knowledge of human anatomy and physiology Familiar with medical terminology and practices Attention to detail with good research skills Possess excellent project management, coordination and organizational skills Excellent communication skills with ability to work in a team Proficient in basic computer and software applications

Employment History: Illinois General Hospital, Illinois June 2005 till date Clinical Research Coordinator      

Maintain protocol requirements for patient visits, patient visit schedules, blood draw, test procedures, and drug accountability requirements Complete all study documentation forms like case report forms and other specific research documents Conduct patient care visits and assure that all the procedures are performed in compliance with the standard of the hospital Interact with investigators to assure that the patient receives appropriate medical evaluation and care, when needed Interact with clinical research associate to facilitate monitoring and database clean-up process Attend meetings and conduct clinical research in compliance with all the applicable regulations


Institute of Health Sciences, Illinois April 2003 to December 2004 Clinical Research Coordinator       

Assign tasks of developing and preparing clinical research protocols Responsible for organizing all aspects of medical research project of the organization Coordinate the functions of different departments who work for clinical trial in investigating new health care terminologies, medicines, and procedures Handle the responsibilities of managing investigation devices and maintaining database of the project Perform clinical trial preparation like planning, assembling and instructing clinical trial team Ensure that the medical professional that participates in the clinical research is qualified to fulfill the assigned duties Handle responsibilities of conducting clinical trials of clinical research staff

Educational Summary: Achieved master’s degree in Public Health University of Illinois in the year 2003 Achieved bachelor’s degree in Public Health College of Medical Sciences, Illinois in the year 2000 Certification: Certified Clinical Research Coordinator, Illinois Personal Details: Name: Paul Smith Date of Birth: 13/01/1978 Employment Status: Full time Relationship status: Single Reference: Will be pleased to furnish upon request


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