
Medical Study Coordinator
23 hours ago
Job Overview:
The position of Clinical Research Coordinator involves ensuring the smooth operation of research studies in a hospital setting.
Main Responsibilities:
- Participant Engagement: Identify potential participants, explain study objectives, obtain informed consent, and administer questionnaires
- Data Collection and Management: Retrieve data from electronic health records, set up investigator files, and maintain accurate records using systems like Redcap
- Research Documentation and Administrative Tasks: Prepare documentation for audit purposes, coordinate Institutional Review Board (IRB) applications, and submit annual reports
- Collaboration with Investigators and Clinicians: Establish clinical workflows, prepare necessary documents, and adhere strictly to research protocols
Essential Qualifications:
- Bachelor's Degree in Science, Public Health, or Social Science
- Satisfactory communication and interpersonal skills
- Proficiency in Microsoft office applications
A strong team player with excellent organizational skills is desired for this role. The ideal candidate will possess good problem-solving abilities and be able to work independently in a fast-paced environment. A passion for delivering exceptional results and contributing to the advancement of medical knowledge is essential for success in this position.
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