Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
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.
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