Clinical Research Coordinator

Sun Research Institute is a trusted, independent, multi-specialty research facility located in San Antonio, TX. With nearly 30 years of dedicated service, we are committed to providing study sponsors with high-quality clinical research and reliable patient enrollment across various therapeutic areas. Role Description Under general supervision, the Clinical Research Coordinator provides assistance to the Research Department, including recruitment, managing data, and collecting, processing, and coordinating samples, specimens, and information. Responsibilities Provide assistance to Research staff by organizing files, projects, information and data Collect, process, and assist in the compilation and verification of research data, samples, and/or specimens (following strict protocol and detailed instructions) Enter data from forms and documents into databases and other documents Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol Become familiar with Research SOPs and study protocols Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient Collect, process, and ship blood/urine/stool specimens at patient visits Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Submit patient requests at the conclusion of study visits Ensure the filing and maintenance of all regulatory documents Maintain temperature logs Order and distribute dry ice as needed Periodically check expiration dates on clinical supplies and re-order as needed Assist coordinators with preparation of source documents Assist with subject recruitment by performing chart reviews, cold calling, etc. Process Lab specimens Assist with vital signs Perform Fibroscans once trained Provide general office support to keep operations running smoothly Other duties as assigned Education & Experience Completion of Medical Assistant program Minimum two years of experience in a related healthcare position Previous experience with clinical trials a plus Qualifications & Requirements Able to effectively present information and respond to questions from physicians, staff and patients Proficiency in Microsoft Office software preferred, knowledge of EMR systems required Able to function effectively in a team setting Must have critical thinking skills Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals Able to demonstrate consistent professional conduct and meticulous attention to detail Completion of Good Clinical Practice and IATA training required Must be able to work flexible hours as necessary Previous Medical Assistant and/or Phlebotomy experience preferred Must be a self-starter and demonstrate initiative Willingness to learn a must Benefits Dental insurance Health insurance Life insurance Paid time off Referral program Retirement plan Vision insurance #J-18808-Ljbffr