Research Coordinator Clinical
Resume:
Judy Keene
Fort Myers, FL *****
239-***-**** ********@*****.*** Online Digital Resume
Professional Summary
Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 28 years of related experience to a challenging new role. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in clinical research. Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Skills
Study protocols
Specimen collections
Research SOPs understanding
Medication dispensing
Informed consent
Good Clinical Practices
Dependable and Responsible
Flexible and Adaptable
PPE Compliance
Clerical Support
Multitasking Abilities
MS Office
Organization and Time Management
Schedule Coordination
Trial management
Work History
06/2014 to 11/2021
Senior Clinical Research Coordinator
MOORE Clinical Research, Inc. – Brandon, FL
Collected data and followed research protocols, operations manuals and case report form requirements.
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Gathered, processed and shipped lab specimens.
Followed informed consent processes and maintained records.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Maintained compliance with protocols covering patient care and clinical trial operations.
Carried out day-to-day duties accurately and efficiently.
Completed paperwork, recognizing discrepancies and promptly addressing for resolution.
12/2011 to 06/2014
Clinical Research Coordinator
MOORE Clinical Research, Inc. – Fort Myers, FL
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected data and followed research protocols, operations manuals and case report form requirements.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
Collected, evaluated and modeled collected data.
Worked flexible hours across night, weekend and holiday shifts.
Received and processed stock into inventory management system.
Managed team of employees, overseeing hiring, training and professional growth of employees.
06/2007 to 12/2011
Clinical Research Coordinator
Clinical Physiology Associates – Fort Myers, FL
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected data and followed research protocols, operations manuals and case report form requirements.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
06/1995 to 09/2006
Clinical Research Coordinator
South Florida Bioavailability Company (SFBC) – Fort Myers, FL
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected data and followed research protocols, operations manuals and case report form requirements.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Followed informed consent processes and maintained records.
Education
2000
Nursing Assistant: Nursing Assistance
Lee Vocational - Fort Myers, FL
06/1975
High School Diploma
Riverdale High School - Fort Myers, FL
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