Clinical Research Coordinators or CRCs in short are in charge of providing research coordination, along with consulting with co-investigators on appropriate management of participant problems and concerns. In addition to that they are highly responsible of conducting clinical trials.

Example of Resume for Clinical Research Coordinator

9841 Downtown Abbey, Juneau, AK 56201
(986) 901 – 1126, Email

Seeking a full-time Clinical Research Coordinator-CN2 position at the Massachusetts General Hospital (GHC). Strongly interested in conducting research in an ethical and safe manner.

• Over 5 years of experience in establishing a validation and Q/A process for data integrity and security
• Hands on experience in maintaining and pre-processing data for analysis & interpretation
• Comprehensive knowledge of ensuring proper storage, linkage and cleaning of collected health data
• Professional approach in supporting data verification
• Highly skilled in conducting large mailings
• Track record of maintaining clinical study subject information including survey data
• Well acquainted with assisting program designs and maintenance of survey instruments alongside research consultants
• Complete understanding of administering surveys to study participants as directed
• Skilled in contributing in the development of new surveys and strategies for various programs
• Expert in securely maintaining e-mail addresses for study subjects and use them to send updates

• Self-confident and rational
• Above average computer knowledge
- MS Excel
- MS Word
- Power Point
• Fluent in English and good command over Russian

• Monitored the research so that it follows proper clinical practices
• Proved periodic documentation of the informed consent process for each study subject accurately
• Developed programming of online data collection, surveys and feedback protocol
• Evaluated methods for planning successfully at UMC

06/2007— 07/2012
Union Memorial Clinic – Charlottesville, VA
Clinical Research Coordinator
• Provided oversight and management for DoD human research studies
• Delivered results to stakeholders
• Provided comprehensive planning, direction and leadership to the staff members
• Saw that all the adverse experiences are correctly reported and documented
• Checked the completeness and accuracy of the case reports
• Managed and coordinated proposal and contract needs to meet the department’s goals

State University of Sciences – Streamwood, IL| 2006
B.Sc. (Hons) – Bachelor of Science in Biology
• GPA 3.59

• Cardio-Pulmonary Resuscitation (CPR) |2007
• Dual Energy X-ray Absorptiometry (DEXA) |2007