Clinical Research Coordinator/LPN/RN Apogee Clinical Research, LLC Huntsville, AL Job Details Full-time 1 day ago Benefits Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Life insurance Qualifications Microsoft Outlook Interpersonal skills Spreadsheets Attention to detail Clinical information systems Organizational skills EMR systems Patient interaction Associate's degree Medical terminology Cross-functional communication Full Job Description Apogee Clinical Reseach is growing by filling a Clinical Research Coordinator position with an extremely detail-oriented, highly motivated, well-organized, and personable individual. Are you someone with a medical background who is looking for a future in clinical research? To be successful in this role, you must have a minimum of 2 years of comparable or related medical experience, have strong organizational skills, keen attention to detail, and be an excellent communicator and team player. Extensive knowledge of Medical Terminology is required. Proficiency in Microsoft Office including Excel, Word, and Outlook are required. You must be someone who is able to work in a team that values communication, embraces challenge, and continuous improvement. We're looking for someone who works hard and loves to have fun, is fast-paced and displays a can-do attitude. If this is you and you can prove it, you could be a great fit for our team. This position will be based in Hazel Green, AL, but training will take place at our offices in downtown Huntsville. Applicants need to have reliable transportation. The Clinical Research Coordinator is responsible for the following: Coordinate the day-to-day activities of assigned clinical research studies. Review and implement study protocols, informed consent documents, and other study-related materials. Screen, recruit, and enroll eligible study participants according to protocol requirements. Obtain and document informed consent in accordance with regulatory and institutional requirements. Schedule and coordinate participant visits, procedures, laboratory testing, imaging, and other study activities. Maintain accurate and complete source documentation and study records. Collect, enter, and verify clinical research data in electronic data capture (EDC) systems and other study databases. Track study milestones, participant enrollment, visit schedules, deviations, and follow-up activities. Communicate with principal investigators, sub-investigators, sponsors, CROs, laboratories, and other study partners. Prepare for and support monitoring visits, audits, inspections, and study closeout activities. Coordinate investigational product or study supply accountability when applicable.

Job Type:

Full-time Benefits:

401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance

Education:

Associate (Required)

Experience:

EMR systems: 2 years (Required) patient-facing clinical: 2 years (Required)

Work Location:

In person