Paschal Benard
Senior Clinical Research Associate @Emerald Clinical
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WORK HISTORY
Senior Clinical Research Associate @Emerald Clinical
TX, US
Travelling CRA, successfully managing day-to-day activities of assigned early and late phase clinical trials, exceeding study metrics and completion goals, including trip report submissions.• Monitored investigator sites with a risk-based monitoring approach, applied root cause analysis (RCA), critical thinking, and problem-solving skills to identify site process failure and corrective/preventive actions to bring the site into compliance and decrease risks.• Documented observations in reports and letters promptly. Escalated observed deficiencies and issues to clinical management expeditiously and followed all issues through to resolution.• Facilitated study-related document development, including ICF templates, TMF plans, and essential document lists, ensuring site audit readiness.• Spearheaded site communication and maintenance deliverables to meet timelines.• Provided coaching and training to junior CRAs, fostering their professional development and team success.• Conducted site initiation visits and monitoring visits, training site personnel, identifying potential issues, and ensuring protocol adherence.• Assessed data documentation, reports, and records for accuracy and consistency with CRF and study objectives.• Provided oversight and insights into trial activities (compliance, enrollment, data quality) to PIs, study sponsors, and leadership teams.
EDUCATION
University of Cincinnati
Master of Science - MS, • Master of Pharmaceutical Science in Drug Development (
Imo State University
Bachelor of Science - BS, Computer Science
ABOUT PASCHAL BENARD
At George Clinical, our team has excelled in managing clinical trials, where I have applied my expertise in protocol compliance and IP accountability. With a Master of Science in Drug Development, my focus has been on ensuring study metrics are not just met but exceeded. The use of a risk-based monitoring approach has been instrumental in maintaining high standards of investigation product accountability and source data verification, reflecting our commitment to excellence in clinical research.Our collaborative efforts have contributed to the prompt documentation and resolution of site issues, ensuring compliance and enhancing study integrity. My background in computer science, combined with my clinical experience, empowers me to develop innovative solutions and streamline study-related processes. These competencies, along with my dedication to advancing clinical research, form the cornerstone of our team\'s success in driving forward meaningful scientific inquiry and patient care.
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