Lead global pharmacovigilance initiatives, ensuring compliance and operational excellence while guiding teams through complex safety reporting challenges across diverse therapeutic areas and trial phases.

Lead and oversee clinical research activities across multiple sites, ensuring compliance and efficient operations throughout all study phases while collaborating with site staff to drive success in oncology research projects.

Empower the clinical site management team from initiation to closure, ensuring effective monitoring and sponsor engagement. Drive results while fostering a collaborative and professional environment, meeting project deliverables and budget expectations.

Manage complex clinical trials from initiation to completion, ensuring project success through effective coordination, communication, and teamwork across diverse functional areas and stakeholders. Drive project deliverables within established time, quality, and cost parameters.

Contribute to clinical trial success by leading risk management and central monitoring activities. Collaborate with cross-functional teams to ensure compliance with ICH GCP guidelines and enhance quality throughout the trial lifecycle.