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Clinical Research Coordinator

2 months ago

Mobile Alabama, United States Southern Cancer Center Full time
Job Summary

We are seeking a highly skilled Clinical Research Coordinator to join our team at Southern Cancer Center. The successful candidate will be responsible for supporting the management and coordination of clinical research studies, ensuring compliance with regulatory requirements and maintaining high-quality research practices.

Key Responsibilities
  • Screen potential patients for protocol eligibility and present trial concepts and details to patients, participating in the informed consent process.
  • Assist with patient care in compliance with protocol requirements, including the disbursement of investigational drugs and maintenance of investigational drug accountability.
  • Participate in data collection, entry, and reporting for subjects, reviewing patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
  • Collaborate with physicians to thoroughly document all findings and participate in required training and education programs.
  • May work directly with sponsors, participate in scheduling monitoring and auditing visits, and interact with monitors/auditors while onsite.
  • Assist with the collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations.
  • May be required to complete Hazmat and/or IATA training.
Requirements
  • Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
  • Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology required.
  • Excellent communication, organizational, and time management skills.
  • Strong ability to multi-task and work in a fast-paced environment.
  • Must have a high level of attention to detail and be able to work in a traditional office environment.