Clinical Research Assistant
About The Position
The primary duties of the Temporary Clinical Research Assistant (CRA) include coordinating and processing the administrative and regulatory paperwork associated with ongoing and new Cardiology clinical research trials. Duties include recruiting and consenting patients, attending off-site study meetings as required, scheduling and completing subject follow-up visits, sample processing, attending study teleconferences/training, facilitating investigator and trials personnel training, performing data abstraction and completion of CRFs, adverse event/outcome monitoring and reporting, maintenance of subject research charts, and facilitating study monitor visits. Additionally, the Clinical Research Assistant will track subject visits and site payments, prepare and submit site invoices, utilize complex tracking and budgeting tools to enable accurate forecasting and reconciliation of site and subject payments. This position may assist in preparation of documents required for IRB initial and continuing review (IRB application, consent & HIPPA forms). The CRA will prepare and submit regulatory documents as required by trial sponsor.
Requirements
- On-site, in-person work required
Responsibilities
- Coordinating and processing administrative and regulatory paperwork for clinical research trials
- Recruiting and consenting patients
- Attending off-site study meetings
- Scheduling and completing subject follow-up visits
- Sample processing
- Attending study teleconferences/training
- Facilitating investigator and trials personnel training
- Performing data abstraction and completion of CRFs
- Adverse event/outcome monitoring and reporting
- Maintenance of subject research charts
- Facilitating study monitor visits
- Tracking subject visits and site payments
- Preparing and submitting site invoices
- Utilizing complex tracking and budgeting tools for forecasting and reconciliation of site and subject payments
- Assisting in preparation of documents for IRB initial and continuing review
- Preparing and submitting regulatory documents as required by trial sponsor
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What This Job Offers
Career Level
Entry Level
Education Level
No Education Listed
