Provide a top-quality resume to give yourself the best chance at landing a desired position. While your content is extremely important, the way it is presented is just as vital. A professional Research Associate resume template highlights your abilities and the template below is a great start to landing any job.
Resume Template for a Research Associate
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.
• 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