senior research coordinator resume example with 6+ years of experience
Skilled Clinical Research Coordinator with nursing background and additional certification in IV placement, phlebotomy, HIPPA and GCP certification. Skilled in applying clinical research regulatory requirements such as GCP and ICH guidelines. Proven ability to manage multiple studies simultaneously from inception to completion. Collaborative team player acting as key resource to colleagues. Team leader with ability to train, supervise, motivate, and evaluate. Excellent communication and organizational skills. Over 15 years experience in medical field.
Coursework in Psychology
Diploma in Nursing
Certified in Good Clinical Practice 2013
Medical Interpreter Certificate 2010
Certified in Biological and Environmental Sample Collection and Shipment (IATA) 2009-2010
Certified in HIV/AIDS Education 2008
RASCAL Systems 2006
IV Tech Certificate 2006
LPN permit 2006-2007
Personally recruited, screened and consented over 100 participants.
Delivered compassionate care to study participants that exceeded company requirement.
Instructed and trained new study sites and new stuff on procedures, organization, management, recruitment techniques and importance of cultural sensitivity to guarantee consistent quality of care in accordance to GCP.
Attended several sponsor meetings and implemented new knowledge into routine procedures.
Nominated to the National Society of College Scholars 2012
Named to the University College Dean's List 2011-2013
Lufkin, TX, 08/2010 - 01/2011
- Assist the PI in obtaining and updating all site-specific study requirements including IRB submissions, updates and revisions. Manage the investigation process to ensure compliance with regulatory issues, protocol requirements and GCP: data collection and entry, maintenance of source documents.
- Recruit, screen, consent, randomize and followed patients into clinical trials. Maintain communication with medical monitors, labs, IVRS, ERT on subject reports and visits conducted chart reviews and prepare documentation.
- Coordinate 5-7 research projects to ensure compliance with all regulatory, institutional, and departmental requirements. Ensure that all study subjects are followed with strict adherence and are compliant to the study protocol.
- Serve as a liaison between investigators and study sponsors. Identify and analyze discrepancies in data and regulatory documents to ensure consistency and accuracy. Develop and maintain research schedules, calendars to facilitate data collection.
- Collect, prepare, process, ship and store protocol specimens using universal procedures. Manage data collection and InfoEd data entry, maintain data bases and complete Case Report Forms (CRF) as required
Columbia, MO, 2008 - 08/2010
- Recruited, screened, consented, randomized and followed patients into clinical trials. Supervised 2-3 research staff members and volunteers. Instructed and trained new stuff members on all aspects of study procedures.
- Determined research staffing needs to ensure appropriate coverage and recommend necessary changes to staffing patterns as needed; prioritize and schedule work activities to ensure that workflow is controlled and effectively delegated; identified and resolved staffing issues and shortages by reassigning staff to projects as needed
- Administered structured and semi-structured patient interviews both in-person and over the telephone; conducted reviews of confidential medical records; collected and maintained source documentation of patient records. Developed and maintained research databases and tools (e.g., schedules, calendars, tracking logs etc.) to facilitate data collection. Coordinated all the day-to-day aspects of the study related procedures; assist with schedule of research activities
- Scheduled and coordinated appointments with study participants. Conducted interviews using standardized questionnaires with study participants and instruct participants on self-collected sample and assessment procedures. Collected biological and environmental samples. Conducted anthropometric measurements including skin fold, weight, height, hip and waist circumference and vitals. Prepared forms, supplies and equipment needed for participant home visits. Processed specimens (centrifugation of plasma/serum), and shipped biological samples to the NCS repository. Performed data entry using NCS Information Management Systems (IMS). Calibrated equipment for physical measures. Maintained inventory.
City, STATE, 05/2006 - 05/2007
- Scheduled and coordinated appointments with study participant. Coordinated all the day-to-day aspects of the study related procedures, assisted with schedule of research activities. Ensured that all study subjects are followed with strict adherence and are compliant to the study protocol
- Placed IV for infusions and performed OGTT testing. Performed blood draw and specimen collection. Processed blood specimens (centrifugation and aliquot). Collected, prepared, processed, shipped and stored protocol specimens using universal procedures.
- Performed EKG. Recorded vital signs. Maintained study records.
City, STATE, 2004 - 05/2006
- Scheduled patient appointments and procedures. Reviewed and prepared charts for the visit. Recorded vital signs. Performed EKG, phlebotomy, vaccinations, injections, PT/INR, BS, urine dipstick, urine pregnancy test. Administered oxygen and nebulizer. Assisted in biopsies and minor surgeries.
- Documented health records.
Knowledge of all aspects of study research coordination and monitoring.
Clinical trial audit preparation and corrective action planning. Microsoft Office. Fluent in Russian.
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Resume Overview
School Attended
- Adelphi University
- Adelphi University
- College of Staten Island
- Medical College
Job Titles Held:
- Senior Research Coordinator
- Data Collector/Senior Medical Researcher
- LPN/ Research Worker
- Senior Medical Assistant
Degrees
- MPH
- B.A
- Associate of Science
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