Clinical Research Coordinator - Must be local to Lexington, KY! This is NOT Remote!
About the position EyeCare Partners is the nation's leading provider of clinically integrated eye care. Our national network of over 300 ophthalmologists and 700 optometrists provides a lifetime of care to our patients with a mission to enhance vision, advance eye care and improve lives. Based in St. Louis, Missouri, over 650 ECP-affiliated practice locations provide care in 18 states and 80 markets, providing services that span the eye care continuum. This is a full-time, long-term position. Unfortunately, we cannot accommodate students looking for a summer job or that would need to go part-time during the school year. Responsibilities • Provide clinical research support for studies involving human subjects including administration, project implementation, meeting support, quality assurance, and dissemination of results. • Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments. • Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements. • Support and assist Research personnel in the operation of equipment used in clinical trials. • Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers. • Assist with case management activities to support the work of the project. • Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations. • Assist with the preparation of project reports for PI review and approval. • Support the process of summarizing and sharing project information with other sites. Requirements • High School Diploma or GED equivalent required. • At least one (1) year of experience collecting information using methods such as telephone/face-to-face interviews. • Favorable result on background check required. • Must be able to provide proof of identity and right to work in the United States. • Working knowledge of medical terminology, anatomy, and disease processes. • Demonstrated interpersonal, communication, and interviewing skills with people of all ages. • Organized, detail oriented, self-directed, and dependable. • Able to prioritize work, solve problems, and work independently. • Able to function in a team environment and use negotiation skills. • Able to use computers and software programs for complex tracking of participant tasks. Nice-to-haves • Experience in health research or research data collection. • Familiarity with classification of disease processes. • Undergraduate degree in a related field. • Knowledge of basic research ethics and principles. • Skilled in working with Word, Excel, PowerPoint, and basic knowledge of computer functions. Benefits • Full Benefits Package - Medical, Vision, Dental and Life Insurance • 401k + Employer Matching • Paid Time Off (PTO) and Paid Holidays • Paid Maternity Leave • Employee Discounts • Competitive Base Pay Apply tot his job