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Limited Term Clinical Reserach Coordinator
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DelRicht Research
Central, LA (In Person)
Full-Time
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Job Description
Limited Term Clinical Reserach Coordinator DelRicht Research - 3.5 Central, LA Job Details Full-time 20 hours ago Qualifications Direct patient care Care documentation Mid-level Schedule management Bachelor's degree Clinical documentation Implementing research protocols Medical Assisting LPN Medical assisting 1 year Clinical trial support in drug product development Time management Immunizations Full Job Description Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you! Who We Are DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states. DelRicht Research has been recognized as a Top Workplace for 2023, 2024, 2025, and 2026!! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction. Limited Term Clinical Research Coordinator's Main Objective Overall, the Clinical Research Coordinator is responsible for supporting vaccine clinical trials while delivering excellent patient care, maintaining protocol compliance, and flexing into broader site operations as needed: Support clinical research visits across multiple studies in a clinic setting Prepare study medication and coordinate handoff to the blinded team as needed Help create structure and stability during busy or changing visit schedules Follow study protocols, clinic processes, and documentation expectations accurately Communicate clearly with teammates and help the team adapt when priorities shift Maintain professionalism, timeliness, and reliability in a fast-paced clinical environment Skills needed to win At least 1 year of professional work experience Comfort working in a clinic environment and learning clinical research workflows Strong time management, reliability, and follow-through Tech-savvy and comfortable learning new systems Ability to take direction, stay organized, and support a team through changing priorities A professional, flexible, and team-oriented approach Medical Assistant certification, LPN background, or similar healthcare training Bachelor's degree or equivalent experience, especially for candidates without a clinical certification or licensure Experience supporting patient visits, clinical operations, or healthcare documentation Interest in clinical research, healthcare, or a future medical career The Right Candidate Will Be self motivated! Energetic! Positive! Bring professionalism, maturity, and strong personal accountability to a fast-paced clinical environment Balance unblinded study responsibilities with the ability to support broader CRC work across general medicine and other site needs Be highly dependable and able to maintain focus in a role that requires precision and trust Be remarkably organized Be skilled at problem solving, planning and being proactive Accept ownership of tasks from inception through completion and assume responsibility for personal success