Clinical Research Coordinator II: Drive Data & IRB Studies

UMass Chan Medical School; Worcester (MA); On-site; USD 65,000 - 85,000; Full time

Job summary

University of Massachusetts Chan Medical School invites applications for a Clinical Research Coordinator II to support complex human subject research. The role involves independent task execution under the PI, regulatory coordination, data management, and contributions to study tools and literature resources.

Responsibilities include obtaining consent, scheduling visits, ensuring accurate regulatory documentation, QA of data, and assisting with grant/contract financials.

Qualifications

• Bachelor's degree in a scientific or health-related field, or equivalent experience.
• 1-3 years of related experience.
• Ability to travel off site locations.

Responsibilities

• Obtain consent of research participants in accordance with IRB approved protocols and all applicable regulations including HIPAA
• Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
• Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
• Conduct preliminary quality assurance reviews of study data
• Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
• Present study status reports related to assigned research projects

Education

Bachelor's degree in a scientific or health related field

Job description

University of Massachusetts Chan Medical School invites applications for a Clinical Research Coordinator II to support complex human subject research. The role involves independent task execution under the PI, regulatory coordination, data management, and contributions to study tools and literature resources.

Responsibilities include obtaining consent, scheduling visits, ensuring accurate regulatory documentation, QA of data, and assisting with grant/contract financials.