Clinical Research Coordinator - Must be local to Lexington, KY! This is NOT Remote!

🌍 Remote, USA 🎯 Full-time πŸ• Posted Recently

Job Description

About the position Responsibilities β€’ Provide clinical research support for studies involving human subjects including administration, project implementation, meeting support, quality assurance, and dissemination of results. β€’ Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments. β€’ Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements. β€’ Support and assist Research personnel in the operation of equipment used in clinical trials. β€’ Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers. β€’ Assist with case management activities to support the work of the project. β€’ Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations. β€’ Assist with the preparation of project reports for PI review and approval. β€’ Support the process of summarizing and sharing project information with other sites. Requirements β€’ High School Diploma or GED equivalent required. β€’ At least one (1) year of experience collecting information using methods such as telephone/face-to-face interviews. β€’ Favorable result on background check required. β€’ Must be able to provide proof of identity and right to work in the United States. β€’ Working knowledge of medical terminology, anatomy, and disease processes. β€’ Demonstrated interpersonal, communication, and interviewing skills with people of all ages. β€’ Organized, detail oriented, self-directed, and dependable. β€’ Able to prioritize work, solve problems, and work independently. β€’ Able to function in a team environment and use negotiation skills. β€’ Able to use computers and software programs for complex tracking of participant tasks. Nice-to-haves β€’ Experience in health research or research data collection. β€’ Familiarity with classification of disease processes. β€’ Undergraduate degree in a related field. β€’ Knowledge of basic research ethics and principles. β€’ Skilled in working with Word, Excel, PowerPoint, and basic knowledge of computer functions. Benefits β€’ Full Benefits Package - Medical, Vision, Dental and Life Insurance β€’ 401k + Employer Matching β€’ Paid Time Off (PTO) and Paid Holidays β€’ Paid Maternity Leave β€’ Employee Discounts β€’ Competitive Base Pay Apply tot his job Apply tot his job

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