Meticulous Certified Clinical Research Coordinator, excellent at juggling multiple tasks and working under pressure. Broad industry experience includes Healthcare, Regulatory submissions and Team Management.
Organized and led weekly staff meetings to ensure proper growth of new coordinators and to review all processes in the department to minimize chances of errors with protocols.
Initiated outreaches to public support systems to improve networks for patient care.
Certified Research Coordinator for over 14 years.
Directed patient flow during practice hours, minimizing patient wait time.
Acted as a liaison between the business department, CROs and third party vendors in maintaining proper protocol training and EDC operations.
Demonstrated knowledge of HIPAA Privacy and Security Regulations by appropriately handling patient information.
Developed patient care plans, including assessments, evaluations, and source forms.
Achieved departmental goals and objectives by instituting new processes and standards in research protocols for mild traumatic brain injury care.
Participated in unit based Quality Assurance Program.
Created and maintained all absentee calendars, research assistant and data analysis programmers schedules and staff meeting minutes.
Acted as patient advocate and implemented total patient care as part of conducting research at the clinic level.
Assisted physicians in focus studies on protocol specific medical indication.
Ensured efficacy of treatments through monitoring of treatment regimens.
Prepared for HIPAA and FDA reviews, ensuring required brochures and pamphlets were available to patients in all clinics.
Maintained all confidential personnel files, licensing and CPR compliance records.
Recorded patients' medical history, vital statistics and test results in medical records.
Performed pregnancy tests and sent specimens for laboratory testing.
Monitored patient reactions to drugs and carefully documented progress of individuals participating in clinical trials.
Served as a liaison between patients and physicians to assist patients in understanding their treatment plans.
Utilized strong assessment skills to determine necessary patient care.
Provided on-call care at all times of day and night.
Measured urine specimens and delivered them to the laboratory.
Prepared specimens for analysis and established proper chronological priorities in testing.
Read and recorded temperature, pulse and respiration.
Completed and submitted clinical documentation in accordance with agency guidelines.
Properly prepared in patient orders for in patient research protocols.
Met enrollment numbers for in-patient clinical trials.
Maintained adverse event records and subject charts.
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