Oncology Pharmacovigilance Director

GlaxoSmithKline; United States; Híbrido; USD 170.000 - 283.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement benefits

Paid holidays

Paid vacation

Descripción de la vacante

GlaxoSmithKline is seeking a seasoned Pharmacovigilance leader for a hybrid role based in the United States. You will drive safety governance, risk management planning, and the safety components of regulatory submissions to ensure patient safety across our portfolio.

The role requires 5+ years in pharmacovigilance, deep knowledge of ICH/GVP, and a proven ability to lead cross-functional teams. The position offers competitive benefits, an annual bonus, and opportunities to influence safety

Formación

• PhD in Life Sciences or related field (PhD preferred)
• 5+ years of pharmaceutical/biotech pharmacovigilance experience
• Experience with safety evaluation, risk management and data from clinical/post-marketing
• Knowledge of ICH, GVP and regulatory requirements

Responsabilidades

• Leads safety governance and risk management planning.
• Leads the safety component of global regulatory submissions.
• Interprets data from literature and clinical studies for safety.
• Manages cross-functional safety teams and expedites issue resolution.
• Ensures risk-reduction strategies are reflected in protocols and labeling.

Conocimientos

Pharmacovigilance

Safety management

Regulatory liaison

Educación

PhD in Life Sciences

Bachelor's in Life Sciences

Descripción del empleo

GlaxoSmithKline is seeking a seasoned Pharmacovigilance leader for a hybrid role based in the United States. You will drive safety governance, risk management planning, and the safety components of regulatory submissions to ensure patient safety across our portfolio.

The role requires 5+ years in pharmacovigilance, deep knowledge of ICH/GVP, and a proven ability to lead cross-functional teams. The position offers competitive benefits, an annual bonus, and opportunities to influence safety