Pharmacovigilance PV-RMP Lead

Baxter International; Deerfield (IL); Presencial; USD 112.000 - 154.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health & dental coverage

ESPP

401(k) plan

Paid time off

Descripción de la vacante

Baxter International Inc. is seeking a Pharmacovigilance Risk Management Specialist to lead the development and maintenance of PV-RMPs, supporting safe use of Baxter products worldwide.

You will collaborate with global partners to ensure regulatory submissions meet health authority requirements, translating complex safety data into clear risk management documents. The role requires scientific/clinical knowledge, strong writing, and attention to detail, with opportunities to mentor and train new

Formación

• Bachelor’s degree in Nursing, Biological Sciences, Medical, Clinical, or related field.
• 2+ years in Pharmacovigilance or related functions.
• 2–3 years authoring PV-RMPs.

Responsabilidades

• Author PV-RMPs using global, regional, local templates.
• Coordinate cross-functional PV-RMP reviews and approvals.
• Respond to regulatory questions and commitments on PV-RMPs.
• Manage timelines, deliverables, and submissions for PV-RMPs.
• Collaborate with country affiliates and global stakeholders on PV-RMPs.

Conocimientos

Analytical thinking

Project management

Communication skills

Regulatory interaction

Technical writing

Educación

Bachelor's degree

Advanced degree

Descripción del empleo

Baxter International Inc. is seeking a Pharmacovigilance Risk Management Specialist to lead the development and maintenance of PV-RMPs, supporting safe use of Baxter products worldwide.

You will collaborate with global partners to ensure regulatory submissions meet health authority requirements, translating complex safety data into clear risk management documents. The role requires scientific/clinical knowledge, strong writing, and attention to detail, with opportunities to mentor and train new