Sharon M. Brown
Mesquite,Tx
Summary
I am a Clinical Research Coordinator with over 2 decades of experience. I possess excellent organizational skills, which have allowed me to manage multiple projects simultaneously while maintaining attention to detail. My interpersonal skills are superb, allowing me to build strong relationships with Investigators, Vendors, and Sponsors alike. Proactive Clinical Coordinator excited to transition into a new position where superb leadership and clinical coordination abilities can be utilized. Skilled in task delegation, staff recruitment and scheduling. Committed to ensuring staff is compliant with all safety and health standards and protocols.
Overview
13
13
years of professional experience
Work History
Clinical Research Coordinator II
Baylor Scott & White Research Institute
Dallas, TX
12.2016 - Current
- Data management; Performs or assists in data entry, configuration, and analysis
- Participate in quality and process improvement efforts to create a high-performing and efficient team
- Guides lower-level personnel involved in the planning, implementation, and evaluation of clinical studies
- Assists in training new personnel.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Gathered, processed, and shipped lab specimens.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
Research — Clinical Research Coordinator II
Dallas Clinical
08.2016 - 11.2016
- Dispense/Account for Investigation Products as well as instruct subjects on usage and potential side effects
- Provide a leadership role in developing, implementing, and evaluating the conduct of studies
- Provides in-service training and serves as a resource to other clinical personnel including physicians, nurses, and other allied health professionals regarding clinical trials, protocols, GCP guidelines, federal regulations, and site SOP.
Clinical Research Coordinator II
Creighton University
Omaha, NE
09.2010 - 08.2016
- Compile Routine reports such as progress and bias reports to ensure studies are executed on time and that quotas are met
- Monitor quality fieldwork and manage multiple projects annually
- Manage and coordinates research project budget development
- Manage and assist with the development of training and educational material for assigned research protocols.
Education
B.S - Business
Bellevue University
Bellevue, NEA.D. Medical - undefined
Omaha College of Health Careers
Omaha, NESkills
- Clinical Quality Improvement
- Unit Leadership
- Managing Patient Cases
- Unit-Based Shared Governance
- Clinical Data Collection
- HIPAA Compliance
- Compliance with Regulatory Guidelines
- Medical Records Management
Timeline
Clinical Research Coordinator II
Baylor Scott & White Research Institute
12.2016 - Current
Research — Clinical Research Coordinator II
Dallas Clinical
08.2016 - 11.2016
Clinical Research Coordinator II
Creighton University
09.2010 - 08.2016
B.S - Business
Bellevue University
A.D. Medical - undefined
Omaha College of Health Careers
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