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The SDTM Programmer leads study-level programming activities, ensuring quality SDTM deliverables for clinical trials and collaborating with cross-functional teams.

The National Director will develop and execute a US thought-leadership engagement plan for Nephrology, collaborating closely with several teams to drive strategic priorities and manage resources.

The Sr. Manager, Global Regulatory Affairs supports regulatory strategy, oversees submissions, manages queries, and collaborates with internal teams and CROs on compliance and implementation.

The Payment Specialist manages investigator payments, ensuring compliance with clinical trial agreements, resolving payment issues, and collaborating with various teams to support clinical trials effectively.

The Associate Director will provide regulatory strategic advice for U.S. communications, ensuring compliance with FDA regulations while collaborating with cross-functional teams to support materials for healthcare providers, payors, and patients.

The Senior Pharmacovigilance Lead manages safety operations, oversees PV resources, ensures compliance, and leads cross-functional safety governance in clinical programs.

Oversee clinical pharmacology plans for drug candidates, lead studies, analyze pharmacokinetic data, and engage with health authorities to guide drug development strategies.