Tomi Taiwo
Senior Clinical Research Associate @IQVIA
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WORK HISTORY
Senior Clinical Research Associate @IQVIA
Key ResponsibilitiesLead site selection, initiation, routine monitoring, and close‑out activities in alignment with study protocols, contracted scope, and Good Clinical Practice (GCP) standards.Develop and support site‑level subject recruitment strategies, partnering closely with sites to adapt, drive, and track recruitment performance to meet project timelines.Manage a diverse portfolio of study sites across multiple therapeutic areas, ensuring high‑quality execution and adherence to protocol requirements.Deliver protocol and study‑specific training to site personnel and maintain consistent communication to manage expectations, address issues, and support ongoing study needs.Assess site performance, data integrity, and regulatory compliance, escalating quality concerns when necessary to safeguard study outcomes.Oversee study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution; contribute to study start‑up activities when required.Maintain comprehensive documentation of monitoring activities, including visit reports, follow‑up communications, and corrective action plans.Mentor and support junior clinical staff through co‑monitoring visits and training sessions.Contribute to the development of study tools, documentation, and operational processes to enhance study efficiency.Communicate study objectives, expectations, and opportunities to site teams to strengthen engagement and performance.Collaborate cross‑functionally with project teams to ensure smooth study execution and alignment across operational activities.
EDUCATION
University of Hertfordshire
Biomedical Science
SKILLS
ABOUT TOMI TAIWO
BSc (Hons) Biomedical Science graduate, with more than 7 years work experience in the pharmaceutical and CRO industry as a Clinical Monitoring Associate, Clinical Trial Specialist, QC technician and a biomedical researcher. Currently working as a Clinical Research Associate, demonstrating communication and organisation skills, whilst liaising with team members and clients to successfully manage phase clinical trials in various indications. Furthermore 5 years work experiences in retail were client satisfaction was achieved every time.
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