Judy Keene
Fort Myers,FL
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.
Overview
26
26
years of professional experience
Work History
Senior Clinical Research Coordinator
MOORE Clinical Research, Inc.
Brandon, FL
06.2014 - 11.2021
- 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.
Clinical Research Coordinator
MOORE Clinical Research, Inc.
Fort Myers, FL
12.2011 - 06.2014
- 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.
Clinical Research Coordinator
Clinical Physiology Associates
Fort Myers, FL
06.2007 - 12.2011
- 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.
Clinical Research Coordinator
South Florida Bioavailability Company (SFBC)
Fort Myers, FL
06.1995 - 09.2006
- 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
Nursing Assistant - Nursing Assistance
Lee Vocational
Fort Myers, FL2000
High School Diploma -
Riverdale High School
Fort Myers, FL06.1975
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
Timeline
Senior Clinical Research Coordinator
MOORE Clinical Research, Inc.
06.2014 - 11.2021
Clinical Research Coordinator
MOORE Clinical Research, Inc.
12.2011 - 06.2014
Clinical Research Coordinator
Clinical Physiology Associates
06.2007 - 12.2011
Clinical Research Coordinator
South Florida Bioavailability Company (SFBC)
06.1995 - 09.2006
Nursing Assistant - Nursing Assistance
Lee Vocational
High School Diploma -
Riverdale High School
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