Clinical researchers need some administrative and research support in order to help them with their work
.They are hired to assist the research staff so that research activities can be carried out without any hitches.
A clinical research assistant usually reports to the manager of clinical services.
Some of the duties of a clinical research assistant include managing the front desk, organizing research files, assisting with research studies and programs, and verifying research data.
The work of people working in this position is mostly clerical in nature although they spend a great amount of time helping with research activities.
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If this work interests you, the following resume sample should interest you as well.
Sample Resume for Clinical Research Assistant Position
Felicity Stone
3031 Shane Way, Reno, NV 66662
(000) 999-3625
Email
CLINICAL RESEARCH ASSISTANT
SUMMARY
Dynamic and extroverted clinical research professional with 9+ years’ hands-on experience in developing and presenting trial protocols and designing data collection forms. Well-versed in liaising with healthcare professionals and setting up clinical trials. Profound know-how of handling filing and collating duties to manage appropriate documentation.
CORE COMPETENCIES
• Medical Terminology
• MS Office Suite
• Medical Chart Abstraction
• FDA regulations
• GCP-ICH
• HIPAA guidelines
SELECTED ACHIEVEMENTS
• Solely handled the development and implementation of strategies aimed at increasing patient randomization in clinical trials.
• Introduced a database system that recorded trail shipment details and ensures confirmation to CRA standards.
• Individually handled and coordinated the activities of clinical study participants.
• Awarded with the Clinical Research plaque following excellence in providing support services.
PROFESSIONAL EXPERIENCE
Clinical Research Assistant
Henry Ford Health System, Reno, NA
Jun 2016 – Present
• Assist with actual clinical research activities by collecting and recording pertinent data.
• Study the gathered data to determine accuracy for trials.
• Prepare grant applications and enter all information in databases.
• Secure and ship clinical specimens in accordance to set protocols.
• Make preparations for monitoring visits.
• Create charts for review of gathered data.
• Summarize research findings and make appropriate presentations.
• Review medical records to ensure completeness and accuracy.
Clinical Research Intern
The University of Nevada, Reno, NA
Jan 2009 – May 2016
• Provided front desk support to the research department.
• Took orders for handling research activities.
• Performed research activities in accordance with the orders provided.
• Study research materials to ensure accuracy and relevance to orders.
• Performed filing and data entry duties.
EDUCATION
Master of Science in Human Sciences
The University of Nevada, Reno, NV – 2008