Research Associates (RAs) play an important role in ensuring the quality of ACRIN’s clinical research. The current increased scrutiny of clinical research makes this role even more important than in the past.
RAs are largely responsible for making certain that:
- Data are collected and reported in a timely fashion
- Data are accurate and correctly reflect the patient’s medical records
- Appropriate documentation is maintained
- All study procedures are performed in compliance with hospital regulations, federal regulations, and good clinical practice
RAs who work on ACRIN trials are invited to get involved in the RA Committee by participating in any of the subcommittees: Education, Quality Assurance, Networking and Communications and Mentorship.
The executive functions of the RA Committee are coordinated by the smaller RA Executive Committee, which facilitates the integration of RAs into the ACRIN organization. The committee chairperson serves as liaison to the ACRIN Steering Committee.