Manager overseeing site activation activities in a dedicated department for IQVIA Biotech. Ensuring team performance and operational excellence with regulatory compliance and quality measures.
Responsibilities
Oversee a dedicated department responsible for delivering high‑quality site activation activities.
Ensure operational excellence, team performance, and compliance with regulatory requirements.
Lead a team that performs site activation activities across assigned clinical research projects.
Set goals and objectives for staff, ensuring quality and compliance.
Oversee training, resource allocation, and continuous improvement.
Requirements
Bachelor’s degree in a scientific discipline or healthcare‑related field preferred.
Typically 3–7 years of relevant experience in clinical research, site start‑up, clinical operations, or related functions.
Proven ability to lead teams, manage performance, and drive operational excellence.
Strong understanding of regulatory guidelines (GCP/ICH) and clinical research processes.
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