Clinical Research Coordinator III
A company is looking for a Clinical Research Coordinator III to support large-scale randomized controlled trials focused on relationship health among Service Members and their families.
Key Responsibilities
Coordinate and execute day-to-day activities of two large-scale randomized controlled trials, ensuring alignment with study protocols and timelines
Develop and maintain protocols, standard operating procedures, and regulatory documentation; prepare and submit IRB materials
Monitor participant recruitment, consent, and retention; maintain detailed documentation and collaborate with the data team on quality assurance
Required Qualifications
Bachelor's Degree
Minimum of 6-8 years of experience in research studies from planning through implementation
Strong understanding of IRB processes, human subjects protections, and regulatory compliance
Experience with data quality procedures and participant follow-up strategies
Ability to obtain and/or maintain a T1 Public Trust with CAC
A company is looking for a Clinical Research Coordinator III to support large-scale randomized controlled trials focused on relationship health among Service Members and their families.
Key Responsibilities
Coordinate and execute day-to-day activities of two large-scale randomized controlled trials, ensuring alignment with study protocols and timelines
Develop and maintain protocols, standard operating procedures, and regulatory documentation; prepare and submit IRB materials
Monitor participant recruitment, consent, and retention; maintain detailed documentation and collaborate with the data team on quality assurance
Required Qualifications
Bachelor's Degree
Minimum of 6-8 years of experience in research studies from planning through implementation
Strong understanding of IRB processes, human subjects protections, and regulatory compliance
Experience with data quality procedures and participant follow-up strategies
Ability to obtain and/or maintain a T1 Public Trust with CAC