Benefits/Perks
- Competitive Compensation
- Great Work Environment
- Career Advancement Opportunities
Job Summary
We are seeking a Clinical Research Coordinator to join our team! As a Research Assistant, you will spend your days working and assisting other researchers in daily tasks, designing and preparing experiments and trials, and ensuring everything done is up to regulatory standards. You will also be gathering data and preparing reports based on research done, performing maintenance on everyday equipment, and following all safety standards each day. The ideal candidate has excellent communication skills, previous laboratory experience, and an excellent eye for detail.
1. Preparing for study initiation
2. Obtaining physician signatures
3. Recruiting subjects
4. Screening and scheduling subjects
5. Getting voluntary subject consent
6. Teaching subjects about protocol expectations for them
7. Performing study/protocol procedures in a detailed, accurate manner
8. Maintaining study files
9. Tracking subjects, avoiding lost-to-follow-up
10. Documenting an adverse event
11. Processing and shipping lab work
12. Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel
13. Completing case report forms (CRF's) for PI review and approval
14. Helping study monitors with CRA corrections
15. Maintaining study-specific supplies
16. Preparing for study closure and archiving
Knowledge of Spanish and /or Phlebotomy Training.
Qualifications
- Previous experience in clinical research setting desired
- Strong communication skills
- Excellent attention to detail