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Click here or scroll down to respond to this candidateCandidate's Name
C L I N I C A L R E S EARCH P ROFESSIONALPHONE NUMBER AVAILABLEEMAIL AVAILABLEChicago, IL Street Address
ContactDynamic Clinical Research Coordinator with a proven track record at Retina Consultants, adept in trial management and patient recruitment. Excelled in ensuring study protocols and documentation requirements were met with precision, showcasing exceptional research experience and interpersonal skills. Successfully enhanced patient engagement and data integrity in high-stakes environments.P r o f e s s i o n a l SummaryS k i l l sTrial management Specimen collectionsSpecimen handling Study protocolsData management Research SOPs understandingInformed consent Participant screeningMedication Dispensing Good Clinical PracticesResearch experience Documentation requirementsScheduling prociency Investigational ProductManagementCLINICAL RESEARCH COORDINATOR IIUNIVERSITY OF CHICAGO Chicago, IllinoisOct 2023 - PresentE x p e r i e n c eReview participants' medical records to track and report adverse events and deviations. Identify, recruit and schedule patients who may be eligible to participate in oncology clinical trials (leukemia) Perform patient assessments by taking detailed clinical history and completing patient data forms Provides patients with study information and obtain informed consent forms Initial liaison between physicians, nurses and laboratory personnel as well as sponsors and monitors Responsible for data management by ensuring it is done in a timely matter Oversee patient follow-up during the duration of the trial period Ordered trial kits and provided patients with study drug if needed HIPPA,CITI,GCP, OSHA and IATA trainingExperience with EPIC, RedCap and Velos systems among others
CLINICAL RESEARCH COORDINATORRETINA CONSULTANTS Columbia, SCAug 2021 - Oct 2023OPTOMETRIC TECHNICIAN/ FRONT OFFICE MANAGEMENTNATIONAL VISION Columbia, SCNov 2020 - Aug 2021HEALTHCARE RECRUITERMEDICAL STAFFING NETWORK Columbia, SCMar 2003 - Oct 2005Assist surgeons with procedures relating to the study protocol Handled informed consent and patient recruitmentReviewed regulations to make sure procedures are completed according to the sponsors specifications Handled intake, documentation and storage of medications delivered to the clinic Participated in trainings, seminars and conferences relating to clinical research Updated patient information including insurance and medical records Coordinated transportation and payment for patients if needed Completed all data entry for the site/ sponsors and uploaded results to the database Adapted to various examination scenarios, remaining personable with patients and staff. Drove compliance with visual merchandising in exam lanes, assessment room and contact lens area. Supported contact lens exams by demonstrating contact lens care and maintaining trial inventory. Entered insurance information to ensure proper benefits and payments Prepared patients medical charts and made referrals if necessary Made adjustments to eyewear if it needed repairScheduled and conducted new employee orientations. Addressed employee relations issues, such as harassment allegations, work complaints, or other employee concerns.Performed searches for qualified job candidates, using sources such as computer databases, networking, Internet recruiting resources, media advertisements, job fairs, recruiting firms, and employee referrals. Provided temporary medical staff for hospitals, prisons, private home care and sitters Handled after hours emergency staffingBACHELOR OF SCIENCE (B.S.) IN BIOLOGYAug 1996 GEORGIA SOUTHERN UNIVERSITY Statesboro, GA, US MASTER OF BUSINESS ADMINISTRATION (M.B.A.) IN HEALTH ADMINISTRATION GPA 3.7 WEBSTER UNIVERSITY Columbia SCEducationReferences available upon requestReferences |
