What are the responsibilities and job description for the Clinical Research Support Specialist position at University Cancer & Blood Center/University Health...?
ARE YOU LOOKING FOR A REWARDING CAREER WITH A GROWING AND DYNAMIC TEAM? CONSIDER UCBC.
At University Cancer & Blood Center, we pride ourselves on listening. On providing hope, guidance, and comfort. On getting up each day and striving to make a positive impact on the lives of patients and their families. From our front-desk staff to our counselors, nurses, technicians and physicians – who’ve chosen to accept their calling, we salute them for their efforts and recognize them as the very special individuals that they are.
DO YOU HAVE WHAT IT TAKES TO JOIN US? IF SO WE’D LOVE TO HAVE YOU!
Job Description:
- Check each patient on the daily Clinical Trial patients list.
- Make sure that all patients are up to date on Inform Consent Forms.
- Check for add on orders at end of day
- Check correct EMR access for monitors
- Coordinate with regulatory, data, and nursing personnel to address study team requests
- Support trial patient visits:
- Access central lab reports and work with PI to complete sign off
- Access EKG reports and work with PI to complete sign off
- Prepare radiology discs for submission
- Safety Reports: Access all safety reports weekly
- Temp Logs: Access all temp logs weekly
- Update Binders:
- Ensure del log is updated with all current Sub.I’s, Nurses, and Mix Specialists. Add new staff as needed.
- Review ICF log to ensure it is updated
- Review all training and make sure every Sub I, Nurse, and Mix Specialist has been training
- Check IRB site and make sure all approvals are printed and filed in binder
- Confirm all correspondence is filed
- Current and outstanding protocol training:
- Follow up on outstanding training and new trainings
- Lab Kit Maintenance:
- Complete inventory on lab kits monthly
- Order new lab kits as necessary
- Destroy expired kits
- Drug Destruction Maintenance:
- Destroy drug as needed
- Log destroyed drug
- Complete regulatory startup documents as needed
- Complete annual review of master regulatory documents such lab normal ranges, CVs, etc
- Miscellaneous Projects; Organizational projects, data projects, etc.
