|Location||New Orleans, LA|
|Date Posted||September 15, 2020|
Job Summary: Looking to hire an individual with a Clinical Research Coordinator background to act as a consultant CRC to a research site conducting a COVID-19 clinical trial. The focus for this CRC will be supporting the recruitment, enrollment and retention efforts for the study. He or she will focus on performing chart review of potential patients and pre-screening those who look eligible. Once the chart has been reviewed, the CRC will pre-screen the patient over the phone to confirm eligibility. In addition, the other main focus of this position will be to perform data entry in the EDC and resolving queries.
Other job duties will include creating/uploading source documents, assisting with IRB submissions, patient visit follow up, e-diary assistance, E-consent updates/maintenance, lab kit assembly, and unblinded pharmacy assistance (no administration or IP handling). Lastly, he or she will perform physician outreach to help raise awareness of this COVID-19 study in the medical community- educating medical providers on the study in increase patient referrals.
The individual in this role must be comfortable jumping in with minimal handholding. This COVID-19 study requires an individual be able to work in a high intensity environment as this is an urgent study. A candidate must have 40 hours of availability.
Duties and Responsibilities:
1. Chart review of patient's medical records
2. Pre-screening patients over the phone
3. Scheduling patients for in-person appointments
4. Creating/uploading source documents
5. Assisting with IRB submissions
6. Patient/Subject visit follow up
7. Protocol/study education
8. E-diary assistance
9. E-consent updates/maintenance
10. Lab Kit Assembly
11. Unblinded pharmacy assistance
12. Collection of study data and entering data into EDC (as well as keep EDC up to date)
a. Resolving queries
13. Any additional recruitment or study efforts deemed necessary by site
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