The Clinical Research Coordinator will coordinate and conduct the day-to-day operations of hematology-oncology ongoing studies. The Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, research team, Institutional Review Board and sponsor. The Clinical Research Coordinator screens, enrolls and follows study patients, ensuring protocol compliance, and effective monitoring of clinical trial subjects. The Clinical Research Coordinator is also responsible for all data and source documentation, adverse event reporting, and maintenance of complete regulatory files.
Ability to efficiently coordinate research activities, including generating study recruitment, intervention, and follow-up report, training study staffs, organizing, prioritizing, and scheduling work assignments.
Excellent organizational, interpersonal, and communication skills.
Proficient in various software programs (including database management [e.g. Access], presentation packages [e.g. PowerPoint], spreadsheets [e.g. Excel], and advanced word processing [e.g. Word]).
Highly detailed and organized.
Excellent work ethic.
Excellent analytical skills
Ability to multi-task and work independently.
Ability to maintain confidentiality in all work performed.
REQUIRED EDUCATION AND EXPERIENCE:
Bachelor’s degree in public health or other science area , or RN with current Louisiana licensure at the time of hire or LPN with current state licensure at the time of hire
Three (3) years’ clinical research experience in conducting research and clinical trials, including recruitment, coordinating research activities.
PREFERRED QUALIFICATIONS:
Master’s degree in, clinical research, or public health preferred.
Certified Clinical Research Coordinator
Clinical research experience in hematology, bleeding and clotting disorders.
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