Paulette Covington
Houston,TX
Summary
Motivated and methodical clinical research professional arranging sites, operations and regulatory functions. Proficient in data capture procedures and action planning. Seeking a dynamic, growth-oriented position.
Overview
2025
2025
years of professional experience
2
2
years of post-secondary education
1
1
Certification
Work History
Sr Clinical Research Associate
Monitor PRN, LLC
Houston, TX
03.2015 - 06.2024
- Conducted site visits to assess data integrity and ensure compliance with study protocols and GCP-ICH regulations.
- Collaborated with cross-functional teams to facilitate project timelines and deliverables.
- Reviewed and verified clinical trial data for accuracy and completeness.
- Provide ongoing training required to ensure project expectations are achieved
- Ensure drug/device compliance
- Track and review regulatory documents and approvals
- Ensure reporting of AE/SAEs
IRB Compliance Administrator
Rice University
- Ensured activities maintained compliance with university policies and federal regulations.
- Review and update departmental policies/procedures
- Perform compliance review for initial, Expedited, Continuing and Amendments ensuring timely approvals.
- Monitor IRB meetings
- Assisted in the development of training materials for PI/ researchers on compliance issues.
- Collaborate with team members for process improvement
Education
Bachelor of Science - Nursing
University of Texas Health Science Center
Houston, TX 08.1988 - 06.1990
Skills
- Clinical trial management
- Regulatory compliance
- Data integrity verification
- Protocol development
- Compliance Monitoring
- Quality Review
- Training and mentoring
Certification
- RN license - Texas Board of Nursing-1990-current
Timeline
Sr Clinical Research Associate
Monitor PRN, LLC
03.2015 - 06.2024
Bachelor of Science - Nursing
University of Texas Health Science Center
08.1988 - 06.1990
IRB Compliance Administrator
Rice University