**Remote Role on East Coast**
Job opportunity with a top biopharmaceutical company that is looking for a CTA to join their team on a 6-month contract with a good possibility for conversion or extension!
Pay Rate: $38-$40/hr
Qualifications:
- Bachelor's degree or nursing qualification is required. Scientific/health care field preferred, but not required
- Minimum 2 years of relevant experience in clinical research (e.g. clinical site, CRO, sponsor or clinical trial vendor) or related field
- Adequate Good Clinical Practice training
- General knowledge of guidelines governing clinical research
Job Description/Skills:
- Facilitate study start up tasks including site feasibility and CDA process
- Collect & collate documents required for EC/IRB/HA submissions
- Generate and/or review clinical documents and reports, including first draft of the ICF
- Develop trackers and reports for study related activities
- Track and review essential documents for site activation
- Initiate investigational product release to sites and track site drug acknowledgments
- Manage systems access for study team (e.g. eTMF, CTMS, EDC, IRT
- Perform document quality checks; process and submit documents to eTMF
Benefits/Perks:
- 401k
- Health Insurance
Please apply here directly if interested but If you are genuinely not interested, is there someone you can recommend?