A resume for Clinical Research Coordinator is a marketing tool with a singular purpose i.e. to get you an interview.
If your resume has so far not earned you a job interview, maybe its time to update it. This document furnishes the employers with your relevant professional information. In your resume, you should focus on your strongest skills and accomplishments.
The question is who will determine which of skills are strongest?
You yourself will do that but not in light of your knowledge rather in line with the prospective employer’s requirements. The best way to grab the reader’s attention is to give them what s/he is looking for.
Get help from the sample below to write/update your resume.
See also: Clinical Research Coordinator Cover Letter Sample
Clinical Research Coordinator Resume Sample 1
Robert Kinsley
433 Hailey Ave ● Irving, TX 54391 ● (006) 555-2222 ● robert @ email . com
❖❖ CLINICAL RESEARCH COORDINATOR ❖❖
SUMMARY
A CCRP certified professional offering 6+ years of experience in clinical research coordination. Demonstrated ability to support the management and coordinate the tasks of multiple clinical research studies. Expert in liaising with different departments. Special talent for creating and maintaining databases and reports.
AREAS OF EXPERTISE
| Project Planning | Clinical Data Collection | Data Capture Enhancement |
| HIPPA Compliance | Case Report Development | Internal IRB Administration |
| GCP and GLP | MLS Insurance | Study Feasibility Assessment |
| Network Management | Q/A Data Integration | Clinical Study Monitoring |
KEY ACCOMPLISHMENTS
• Enhanced clinical research accuracy by 30% through the implementation of effective, contemporary clinical research methodology and data collection/validation strategies
• Supervised clinical education and research quality program for one year effectively working with a team of 4 clinical researchers
• Served as study coordinator for 6 months effectively to monitor and facilitate research studies
• Developed and implemented informed consent documentation guidelines
PROFESSIONAL EXPERIENCE
Baylor College of Medicine, Irving, TX | August 2010 – Present
Clinical Research Coordinator
• Initiate, manage and monitor various clinical research projects and provide project specific administrative support
• Schedule and participate in monitoring and auditing activities
• Conduct independent study coordination and screen potential patients for protocol eligibility
• Assist program designs and maintain survey instruments alongside research consultants
• Administer surveys to study participants as directed
Practice plus, Irving, TX | May 2007 – July 2010
Clinical Research Intern
• Oversaw and implemented daily operational aspects of clinical research
• Worked closely with clinical trial sponsors for site assessment, qualification and initiation visits
• Ensured research protocol compliance while subjects were at work
• Contributed to the development of new surveys and strategies for various programs
• Securely maintained e-mail addresses for study subjects and used them to send updates
EDUCATION
TEXAS COLLEGE OF MEDICINE, Irving, TX – 2007
BS, Clinical Coordination
Clinical Research Coordinator Resume Sample 2
CARTER GIBSON
9841 Downtown Area ● Juneau, AK 56201 ● (000) 901 – 1126 ● Email
OBJECTIVE
Seeking a position as a Clinical Research Coordinator at the Massachusetts General Hospital (GHC). Strongly interested in conducting research in an ethical and safe manner.
HIGHLIGHTS OF QUALIFICATIONS
• 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
KEY ACCOMPLISHMENTS
• 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
EMPLOYMENT HISTORY
06/2007— 07/2012
Union Memorial Clinic – Charlottesville, VA
Clinical Research Coordinator
• Provided oversight and management of 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
EDUCATION
State University of Sciences – Streamwood, IL | 2006
B.Sc. (Hons), Biology
• GPA 3.59
CERTIFICATIONS
• Cardio-Pulmonary Resuscitation (CPR) |2007
• Dual Energy X-ray Absorptiometry (DEXA) |2007
OTHER SKILLS
• Self-confident and rational
• Computer: MS Excel, Word, PowerPoint
• Bilingual: English, Spanish