A full-time Research Coordinator is needed at the Nehme and Therese Tohme Multiple Sclerosis Center.
Ensure the accurate execution of research protocols in accordance with Good Clinical Practices and required obligations to patient/subject, Principal Investigator, research team and the sponsor. The Research Coordinator will directly interface with patients/subjects, research participants, and the Principal Investigator in support of the clinical trials and clinical research studies.
Assist with the preparation of IRB applications. Assist with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study.
Gather information from the medical record and physician. Create and maintain participant charts and coordinate participant appointments. Collect, organize and maintain source documentation. Ensure protocol is being followed as approved by the IRB.
Interact with patient/subject and families in a courteous and professional manner. Be consistent and regularly follow through with your patients/subjects reminding them of visits and compliance. Extend this courteous and professional manner to faculty and staff.
Previous experience in coordinating clinical trials is required
Excellent interpersonal, writing, and verbal communication skills in Arabic and English
Experience in working with diverse populations
Must be able to work and make decisions independently
Expertise in understanding and managing clinical study documentation
Be involved in clinical trials organization, facilitating the research process in studies, and coordinating therapeutic trials
Perform other work related duties and complete projects as assigned.
Master's degree preferred
Please submit your CV and cover letter to email@example.com
Only qualified applicants will be contacted back