Katherine Athime
Tampa,FL
Summary
Goal-driven Healthcare Administration professional well-versed in recruiting, training and managing employees to provide exceptional resident services. Highly organized and hardworking with excellent planning and program management skills. 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 19 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. Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation.
Overview
19
19
years of professional experience
1
1
Certification
Work History
Director of Clinical Research, Southwest Florida C
Southwest Florida Clinical Research Center
Tampa, FL
12.2011 - Current
- Set clear, compelling goals for staff and monitored productivity and output for research personnel.
- Thought operationally and displayed communication and leadership skills to follow through on development plans.
- Worked with finance department and built accurate financial statements for clinical research and fostered enterprise-wide view of financial impact of clinical research.
- Recruited, hired and trained all staff, providing direct supervision, ongoing staff development and continuing education to employees.
Clinical Research Coordinator/ IV Therapy/Lab Tech
Eagle Applied Sciences
Biloxi, MS, Kessler Air Force Base, MS
04.2010 - 11.2011
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Followed informed consent processes and maintained records.
Recruiting Coordinator Hired for Recruiting
Mima
Melbourne , FL
10.2009 - 04.2010
- Operated and maintained applicant tracking and candidate management systems.
- Meet my enrollment and exceed the enrollments.
Clinical Research Coordinator IV Therapy/Lab Tech
Lovelace Scientific Resources -
Chipley, FL
09.2009 - 04.2010
- 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.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Clinical Research Coordinator
Rheumatology Associates Of Central Florida
Orlando, FL
03.2007 - 09.2009
- 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.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Clinical Research Coordinator/Phase I
SFBC
Fort Myers, FL
06.2004 - 09.2007
- 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.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
- Gathered, processed and shipped lab specimens.
- 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
- Collected, evaluated and modeled collected data
- Monitored unit budget to meet financial objectives for spend rate and funding
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols
Education
Associate of Applied Science - CMA
03.2005
Associate of Applied Science - Computer Science
09.2000
Skills
- Investigator Meetings
- Research Management
- Department Oversight
- Clinical Trials and Research
- Informed Consent
- Feasibility Studies
- Resource Monitoring
- Facility Inspections
- Clinical Staff Management
- HIPAA Guidelines
- Patient Care Assessment
- Monitoring Visits
- Site Selection
- Trial Close
- Site and Study Management
- Specimen Storage
- Drug Storage Procedures
- Study Coordination
- Regulatory Compliance and Documentation
- Policy Standards and Guidelines
- Processing Specimens
- Team Meetings
- Patient Safety
- Informed Consent Procedures
- Site Investigation Reports
- Site Visits
- Standard Operating Procedures Understanding
- Reading Comprehension
- Product Inventories
- Patient Flow
- Developing Study Tools
- Trial Oversight
- Medidata Rave
- Complex Problem-Solving
- Regulatory Processes
- Laboratory Results Management
- Lab Specimens and Collections
- Good Clinical Practice
- Documentation Requirements
- Specimen Collection
- Study Protocols
- Specimen Handling
- Medical Histories and Vital Statistics
- Customer Satisfaction
- Submission Coordination
- Specimen Coordination
- Phlebotomy
- Patient Care
- IATA
Certification
Certified IV
CMA
Phlebotomy
Timeline
Director of Clinical Research, Southwest Florida C - Southwest Florida Clinical Research Center
12.2011 - Current
Clinical Research Coordinator/ IV Therapy/Lab Tech - Eagle Applied Sciences
04.2010 - 11.2011
Recruiting Coordinator Hired for Recruiting - Mima
10.2009 - 04.2010
Clinical Research Coordinator IV Therapy/Lab Tech - Lovelace Scientific Resources -
09.2009 - 04.2010
Clinical Research Coordinator - Rheumatology Associates Of Central Florida
03.2007 - 09.2009
Clinical Research Coordinator/Phase I - SFBC
06.2004 - 09.2007
Hodges University - Associate of Applied Science, CMA
Southwest Florida College - Associate of Applied Science, Computer Science
Certified IV
CMA
Phlebotomy
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