Seeking Experienced, Clinical Research Coordinator for research company affiliated with Medical aesthetic office in Chicago’s Gold Coast!
The Clinical Research Coordinator will support the research infrastructure, principal investigator, and the research clinic and clinicians, performing diverse clinical research duties while collaborating with with intra-office companies including but not limited to data collection, development and expansion of research databases, contact with external agencies, ensuring research related paperwork is organized and accounted for with technical expertise, recruiting and managing patient and patient data via pre-screening phone and in person interviews as well as completing miscellaneous study tasks assigned by the Principal Investigator and/or the Clinical Director as needed.
Responsibilities and Requirements
Must provide exceptional organization and accurate documentation with attention to detail.
Maintains data for current, accurate and timely status of all case reports, documentation and contacts including phone calls, correspondences, dug dispension, reports and logs, related to research and projects in an orderly efficient method.
Must adhere to highest standards of Confidentiality and HIPAA Compliance while overseeing enrollment and mandatory consents.
Develop a clear and concise plan for recruiting, registering and retaining patients for all current and future clinical trials while keeping and maintaining accurate patient database
Prepares, types, updates and maintains all correspondence, proposals, reports and other documents, related to research and projects, utilizing the computer system and adhering to established deadlines.
Works with Clinical Director of Aesthetic Research to discuss strategies and marketing for eligible patient recruitment. The Clinical Coordinator will be prepared to bring as many suggestions/ideas as possible to the meeting for specified studies.
Transcribe source to CRF’s
Develop and manage photographs and photography protocol for team members.
Must participate and adhere to all division and department policies, procedures and standards, code of Ethics, Good Clinical Practices and Compliance program standards especially those related to research.
Must identify, record and inform investigators of any adverse event or side effect data and assist in resolution efforts according to protocol revisions with oversight companies.
Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Directing drugs and specimens, ie ordering drugs or devices necessary for study completion, dispense to patient as calculated while providing instructions per provisions of study, collection labeling, storage and/or shipment of specimens.
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
About DeNova Research
Clinical Research site in the heart of the Gold Coast area of Downtown Chicago seeking a research coordinator to join our team