Clinical Research Coordinator - Must be local to Lexington, KY! This is NOT Remote!
About the position 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 Apply tot his job