We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized.
We are also open to those looking to relocate to Alabama . If you're a Clinical Research professional ready to take the next step in their career and live in Birmingham !
We are looking for CRC's with over 2 years of experience in clinical research and has previously worked on oncology trials.
HIRING IMMEDIATELY ENT TRIALS CANCER TRIALS - 401K
PTO BENEFITS GROWTH - BIRMINGHAM
RESPONSIBILITIES
1. Coordinates the implementation of multiple complex clinical research protocols.
2. Develops SOPs and templates with guidance from the PI and / or Clinical Research Manager.
3. Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
4. Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
5. Plans strategies to monitor, document, report, and follow-up on unanticipated occurrences
and protocol deviations. Develops and implements preventive / corrective actions.
6. Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
7. Organizes / manages site visits and internal / external auditing activities as assigned.
8. Coordinates research team meetings; assures communications in cross functional teams.
9. Assures synchronization of study visits / procedures / clinical tests with data collection schedules, established time- points;
manages progress of study participants through protocol; expedites overall study progression.
10. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
BENEFITS
- Medical, Dental, Vision insurance
- Commuter Benefits
- 401k with employer match
- Tuition Assistance, Caregiver Resources and more!
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