A proactive and detail-oriented individual with a strong foundation in clinical trial management and regulatory compliance. Skilled in collaborating with internal teams, clinical sites, and vendors to ensure smooth trial execution while adhering to standard operating procedures and good clinical practice. Experienced in coordinating trial activities, tracking program progress, and facilitating clear communication between all involved parties. Adept at organizing meetings, preparing agendas, and managing action items to keep projects on track. Knowledgeable in maintaining trial status records and supporting overall study operations. Actively developing expertise in clinical site monitoring under experienced professionals, with a willingness to travel as needed. A quick learner with a growth mindset, committed to adaptability, teamwork, and contributing to successful clinical research programs.
References available upon request