- Los Angeles, California, United States
- On-site
- Full-time · Entry
- $26–$30 per hour
- 2+ years
Collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies.
Compensation
The hourly pay for this role is $26/hour-$30/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.
Responsibilities
- Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
- Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.
- Review patient data for completeness and accuracy for assigned studies.
- Coordinate and schedule monitor visits for assigned studies.
- Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
Requirements
- High School Diploma/GED
- Bachelor’s degree
- Nice to have: CCRP or CCRC credentials