Research Associate Resume Template

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Resume Template for a Research Associate

Kimberly Jackson

Professional Summary

Knowledgeable Research Associate adheres to Federal regulations and standard clinical trial processes to produce reliable and high-quality results. Adapts to fast-paced trial atmosphere and displays a proven ability to create solutions in flexible situations. Demonstrated communication skills and principles of integrity.

Core Qualifications

• CCRC and SoCRA certification
• Data management
• Microsoft Office, Outlook
• Medical records systems
• Electronic clinical trials databases
• ICH guidelines


Senior Clinical Research Associate/Oncology, January 2011 – present
Clinipace Worldwide – Minneapolis, Minnesota

• Maintained clinical sites and ensured compliance with Clinipace SOPs, local regulations and ICH guidelines
• Developed trip reports and tracked sponsor communications
• Assessed clinical trials for growth and development and coordinated efforts between Lead Clinical Research Team, Trial Manager, Monitor manager and trained monitors
• Assisted with audits and general queries

Clinical Research Coordinator, August 2004 – January 2011
Regions Hospital – Saint Paul, Minnesota

• Coordinated activities with CCRC at Regions Hospital
• Supported emergency medical services, emergency medicine, burn unit and adult/pediatric trauma
• Worked with clinical research manager to conduct clinical trials, recruit test subjects, collect data and maintain file system
• Conducted annual reviews and developed reports on resulting information

Clinical Research Associate, October 2000 – July 2004
Sterling Hoffman Life Sciences – Rochester, Minnesota

• Monitored site management and coordinated with Director of Clinical Studies to achieve satisfactory compliance with company standards and regulatory demands
• Trained, monitored and coordinated incoming staff and oversaw clinical study completion
• Developed clinical study plans that were in compliance with industry standards and created assigned studies issued by company R&D department
• Oversaw the development and creation of clinical study materials, trained and supervised investigators and field staff of various sizes depending on individual studies
• Compiled clinical study data and directed corrections as needed
• Worked with Director of Clinical Studies and department managers to compile final reports and create presentations for CEO and Board of Directors


2000, Master of Science in Clinical Research Administration
Walden University School of Health Sciences – Minneapolis, Minnesota

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