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Clinical Research Coordinator/ Medical Assistant
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Vital Prospects Clinical Research Institute, P.C.
Tulsa, OK (In Person)
$48,696 Salary, Full-Time
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Job Description
Clinical Research Coordinator/ Medical Assistant Vital Prospects Clinical Research Institute, P.C. Tulsa, OK Job Details Full-time $16 - $25 an hour 1 day ago Benefits Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Retirement plan Qualifications HIPAA Records management Attention to detail Health information management Medical terminology Full Job Description Job Overview We are seeking a dedicated and energetic Clinical Research Coordinator/Medical Assistant/CNA/LPN to join our dynamic healthcare research team. We are willing to train. This role offers an exciting opportunity to be at the forefront of clinical trials, contributing to groundbreaking medical advancements. You will coordinate and oversee clinical research activities, ensure compliance with regulatory standards, and provide exceptional patient care and support throughout the research process. Your proactive approach and attention to detail will help drive successful study outcomes while fostering a positive experience for participants. Pay is DOE in the clinical research field. Responsibilities Assist in the planning, organization, and execution of clinical trials in accordance with FDA regulations, ICH GCP guidelines, and institutional protocols. Screen, recruit, and monitor patients or study participants, ensuring adherence to study protocols and maintaining accurate documentation. Collect, review, and manage clinical data, including vital signs, blood samples, and other laboratory specimens, utilizing EMR systems. Conduct patient assessments such as vital signs measurement, blood sampling (phlebotomy), ECG, and recording medical histories using proper medical terminology. Review study documentation for accuracy and completeness; ensure compliance with HIPAA privacy regulations and other applicable standards. Manage data collection processes Ensure all activities comply with Good Clinical Practice (GCP) standards and maintain up-to-date certifications such as ICH GCP certification. Support regulatory submissions by preparing necessary documentation and assisting with audit preparations related to clinical development activities. Experience Bilingual candiates are highly valued for this role. Medical assistant, CNA, LPN, pharmacy technicians encouraged to apply Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques (phlebotomy). Familiarity with EMR systems, data management tools Experience reviewing documentation for accuracy while ensuring compliance with FDA regulations and HIPAA privacy rules. Demonstrated ability to monitor patients effectively while maintaining meticulous records of vital signs and other health procedures.