Clinical Research Coordinator (CRC)

Job Description Job Description Job Description: Clinical Research Coordinator Position Title : Clinical Research Coordinator II Location : Essential Medical Research, Tulsa OK Onsite Employment Type: Full-Time Job Summary : We are seeking a detail-oriented and dedicated Clinical Research Coordinator (CRC) to join our team. The Clinical Research Coordinator is responsible for collaborative support and oversight of assigned clinical research trials to meet accrual targets, facilitate accurate data collection and qualify performance. He/She is the primary point of contact for operational issues during active study conduct. Key Responsibilities : * Study Coordination : * * Manage day-to-day operations of assigned clinical research studies. * Ensure compliance with study protocols, regulatory guidelines, and ethical standards. * Participant Management : * * Partners with treating physician to screen, recruit, and enroll study participants in accordance with GCP Guidelines. * Obtain informed consent and maintain clear communication with participants, CRA, sponsors and physicians throughout the study. * Coordinates patient care in compliance with protocol requirements * May deliver investigational product, drug dairies, perform pill counts and accountability as appropriate * Supports patient teaching regarding administration of investigational product * Document any changes in patient condition, adverse events, concomitant medication use * Address patient reported outcomes as necessary with physicians and other clinical trial staff members. * Data Collection and Documentation : * * Conduct patient visits (Lab draws / EKG's/ conduct patient questionnaires, record, and manage accurate clinical data in electronic or paper-based case report forms (CRFs). * Ensure timely reporting of adverse events and deviations to study sponsors. * Participates in monitoring visits and audits as requested * Participates in required training and education programs * Regulatory Compliance : * * Prepare and maintain regulatory documents, including Institutional Review Board (IRB) submissions. * Conduct study audits and ensure adherence to Good Clinical Practice (GCP) guidelines. * Collaboration and Communication : * * Act as a liaison between study sponsors, investigators, clinical staff, and participants. * Identified quality and performance improvement opportunities and collaborates with leadership in the development of action plans to improve quality * Schedule study visits, coordinate logistics, and facilitate effective communication. Key Competencies : * Strong organizational and time-management skills. * Excellent interpersonal and communication abilities. * Attention to detail and commitment to maintaining data integrity. * Ability to handle sensitive information with confidentiality. * Problem-solving skills and adaptability to dynamic work environments. * Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents and regulatory documents * Demonstrates adaptability: Handles day to day work challenges confidently; is willing and able to adjust to multiple demands, shifting priorities, ambiguity and rapid change; shows resilience I the face of constraints, frustrations or adversity and demonstrates flexibility * Uses sound judgment to make timely, sound decisions under conditions of uncertainty * Shows work commitment: sets high standard of performance; pursues aggressive goals and works efficiently to achieve them. Qualifications : * Degree in a health-related field (e.g., MA/ LPN/ Nursing, Biology, Public Health). * Minimum of 2 years of experience in clinical research field. * Proficient in Microsoft Office Suite (Word/One Note/Excel). Benefits : * Competitive salary and performance-based incentives. * Comprehensive health and wellness benefits. * Opportunities for professional growth and continuing education. * Collaborative and inclusive work environment. How to Apply : Submit your resume and a cover letter to: Jennifer Cleveland View email address on click.appcast.io View phone number on click.appcast.io Include "Clinical Research Coordinator Application" in the subject line. Interested in joining a team that contributes to groundbreaking research that advances healthcare for current and all future generations?