I am a healthcare professional with over 10 years of experience in clinical research, primarily with leading CROs like Parexel and ICON plc. As a Senior Clinical Research Associate, I managed complex dermatology and oncology trials across Phases I-III, ensuring compliance and high-quality data collection. My strong interpersonal skills enable me to build effective relationships with stakeholders. With a Masterʼs in Clinical Trials Monitoring and ongoing studies in Medical Science Liaison, I am committed to driving impactful research and enhancing patient outcomes.
Accountable for conducting monitoring activities of oncology clinical trials in compliance with the protocol.
Handled multiple studies independently while collaborating with teams.
Proactive in identifying, resolving, and escalating project issues.
Conducted site visits and provided support for oncology and pediatric epilepsy clinical trials (Phase I-III).
Developed strong relationships with site staff to ensure regulatory compliance and enhance patient recruitment.
Supported clinical start-up activities management for successful activation timelines.
Acted as the primary liason for investigator sites, overseeing the entire study life cycle for multiple Sponsors.
Conducted monitoring and management of oncology and immunology trials (Phase I-III).
Supported risk management strategies and enhanced trial efficiency.
Accountable for facilitating communication between the Sponsor and research team.
Coordinated observational and cardiology clinical trials (Phase II-III).
Supported enhancement of patient enrollment strategies.
Monitored dermatology trials (Phase II-III).
Ensured compliance with GCP and regulatory guidelines.
Conducted monitoring for oncology and psychiatry observational studies.
Gained hands-on experience in oncology clinical trials, supporting study setup and monitoring activities.