Clinical Research Coordinator Charleston Thyroid Center Mount Pleasant, SC Job Details Part-time $18 - $22 an hour 7 hours ago Benefits 401(k) Flexible schedule Qualifications Teamwork HIPAA Medical scheduling Attention to detail Medical terminology Full Job Description Job Summary We are seeking a dynamic and detail-oriented Clinical Research Coordinator/Clinical Patient Care Coordinator to join our innovative research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring adherence to regulatory standards and ethical guidelines. Your expertise will drive the successful completion of research projects that contribute to advancing healthcare solutions. This position offers an exciting opportunity to work in a collaborative environment dedicated to scientific excellence and patient safety. In addition to coordinating research, you will work collaboratively with our team in coordinating patient care. This includes assistance with prior authorizations, coordinating cancer care, and ensuring that patients receive their medications, scans, and treatments in an organized and efficient manner. We are willing to teach all of these skills to the right applicant and are looking for a highly organized, motivated individual that is a team player and passionate about helping others! We are very flexible with work times and schedules. The right person will be available Tuesdays, Thursdays and Friday AM, ideally. Duties Coordinate and monitor all aspects of clinical trials, including participant recruitment, enrollment, and retention. Review and verify clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards. Conduct patient monitoring activities such as vital signs measurement, blood sampling, and assessment of adverse events. Manage data collection, entry, and management using electronic medical records (EMR) systems and adhere to CDISC standards for data consistency. Ensure compliance with healthcare regulations including HIPAA and clinical ethical guidelines throughout all research activities. Supervise research staff and collaborate with multidisciplinary teams to ensure project milestones are met efficiently. Prepare reports, maintain detailed study documentation, and review clinical laboratory results for accuracy and integrity. Obtain prior authorizations through Cover My Meds or directly with the patient's insurance company. Assist in scheduling patient care, cancer treatments, and imaging procedures. Answer patient questions and inquiries. Skills Proven supervising experience in a clinical or research setting with strong leadership capabilities. Extensive knowledge of medical terminology, clinical research methods, and healthcare compliance standards. Proficiency in data management software. Familiarity with FDA regulations, ICH GCP certification, and clinical trials management protocols. Experience with EMR systems, blood sampling procedures such as phlebotomy, and vital signs monitoring. Strong understanding of clinical development processes, project management in healthcare environments, and research project coordination. Excellent documentation review skills coupled with analysis skills for interpreting complex data sets. Join us in shaping the future of healthcare through rigorous research excellence! We are committed to fostering a diverse environment where innovation thrives and your contributions make a real difference in patient outcomes worldwide. This paid position offers a rewarding career path for passionate professionals eager to advance their expertise in clinical research and patient care coordination while supporting groundbreaking medical discoveries.

Pay:

$18.00 - $22.00 per hour

Benefits:

401(k) Flexible schedule

Work Location:

In person