Clinical Research Coordinator Retina Associates of Cleveland - 3.8 Beachwood, OH Job Details Full-time From $70,000 a year 1 day ago Benefits Health savings account Health insurance Dental insurance 401(k) Flexible spending account Paid time off Parental leave Vision insurance Life insurance Referral program Qualifications Clinical research Biostatistics Research clinical coordinator experience Adaptive clinical trial design Implementing research protocols Productivity software Medical terminology Health informatics Bioinformatics Full Job Description Position Summary Retina Associates of Cleveland, Inc. (RACI), one of the largest retina specialist practices in Ohio, is seeking a motivated, highly organized, and clinically knowledgeable Clinical Research Coordinator to help advance our growing clinical research program across multiple locations. This is an exciting opportunity to join a respected, physician-led retina practice where innovative research and exceptional patient care come together. The Clinical Research Coordinator will play an important role in bringing promising new treatments to patients while helping shape the continued growth of RACI's research program. The position coordinates clinical research studies from start-up through close-out, including patient recruitment and enrollment, study visits, regulatory documentation and compliance, data management, and collaboration with investigators, sponsors, Clinical Research Organizations (CROs), and other research partners. The ideal candidate will bring a strong medical or clinical background, relevant clinical research experience, or a combination of both. We are looking for someone who is detail oriented, adaptable, patient-focused, and excited to contribute to a collaborative team. Experience in ophthalmology or retina research is preferred but not required.

•Competitive compensation based on clinical credentials and relevant research experience

•Essential Duties & Responsibilities Coordinate clinical research studies from start-up through closeout under the direction of the Principal Investigator and RACI leadership. Review study protocols and ensure study requirements and timelines are followed. Identify, recruit, screen, consent, enroll, and follow study participants according to protocol requirements. Coordinate study visits, testing, procedures, and follow-up appointments. Perform clinical assessments and study-related activities within the employee's professional scope of practice and study protocol. Collect, document, and enter study data accurately and resolve data queries as needed. Maintain complete source documentation, regulatory files, and study records. Communicate with investigators, sponsors, CROs, monitors, IRBs, and study participants. Assist with regulatory submissions, monitoring visits, audits, and study closeout activities. Track and report adverse events and serious adverse events according to study and regulatory requirements. Ensure compliance with study protocols, Good Clinical Practice (GCP), HIPAA, FDA regulations, IRB requirements, and RACI policies. Collaborate with physicians and clinical staff to support patient recruitment and integrate research activities into patient care. Assist with developing and improving standardized research processes as RACI's research program grows. Travel between RACI locations as needed. Perform other research-related duties as assigned. Education & Qualifications Required Medical or advanced clinical degree or credential, or equivalent clinical research experience, required. Strong knowledge of medical terminology, patient care, and clinical documentation. Strong organizational, communication, and time-management skills. Excellent attention to detail and ability to manage multiple priorities. Ability to read, understand, and follow clinical research protocols. Ability to work independently and collaboratively as part of a research and clinical team. Proficiency with Microsoft Office and ability to learn electronic research systems. Ability to obtain and maintain required research certifications and training. Reliable transportation and willingness to travel between RACI locations. Preferred Registered Nurse (RN) or Physician Assistant (PA). Active RN or PA license in the State of Ohio. Previous clinical research or clinical trial coordination experience. Ophthalmology or retina research experience. Experience working with sponsors, CROs, monitors, and IRBs. Experience with EDC, CTMS, or electronic regulatory systems. Working knowledge of

GCP, FDA

regulations, and IRB requirements. Current GCP certification. What We're Looking For A dependable, proactive, and patient-focused team member who is excited to help build and grow a high-quality clinical research program at RACI. The ideal candidate takes initiative, communicates effectively, pays close attention to detail, and can adapt as the research program expands across multiple locations. Work Environment This position works within a busy ophthalmology practice and requires regular interaction with patients, physicians, clinical staff, and outside research organizations. Travel between RACI locations and occasional travel for research meetings or training may be required. Equal Employment Opportunity Retina Associates of Cleveland, Inc. is an equal opportunity employer and considers applicants for employment without regard to legally protected characteristics

Pay:

From $70,000.00 per year

Benefits:

401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Parental leave Referral program Vision insurance

Experience:

Clinical research: 1 year (Required)

Work Location:

In person