Clinical Research Coordinator

The Clinical Research Coordinator works under the leadership of the Principal Investigator and/or other Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations.

Requirements

• Bachelor’s degree in a life science or other health professions field
• A minimum of three years of related experience
• Demonstrated computer skills, and proficiency with MS Office Suite software programs
• Excellent written and oral communications skills
• Ability to work evenings/weekends hours as needed
• Knowledge of medical terminology
• Ability to resolve problems/issues
• Strong written and verbal communication skills with the ability to interact with a diverse population of students, faculty, staff, sponsors, and research participants
• Demonstrated organizational and prioritization skills, along with the ability to work in a dynamic environment and to perform multiple tasks simultaneously
• Knowledge of IRB and human subject protection
• Ability to work independently or as a team with excellent attention to detail and adherence to project deadlines
• Ability to travel to off-site locations that may not be accessible via public transportation
• Strong time management skills
• Prior experience with IRB submissions
• Prior experience processing and shipping biological samples
• Prior phlebotomy certification or willing to learn
• Prior experience with RedCap, OnCore CTMS, Epic Research and Florence eBinders
• Prior Electronic Data Capture (eDC) data entry skills
• Prior research experience in a healthcare setting
• Prior research experience with NIH sponsored research studies, industry clinical trials, and investigator-initiated research studies

Benefits

• Full medical, dental, vision coverage
• Paid time off
• 11 Paid Holidays
• Tuition remission
• A generous retirement plan