PV Risk Management Specialist: Lead Global PV‑RMPs

Baxter; Reading; On-site; GBP 50,000 - 70,000; Full time

Job summary

A global healthcare company is seeking a PV Risk Management Specialist in Reading, England. The role involves developing Pharmacovigilance Risk Management Plans (PV-RMPs) and requires expertise in regulatory requirements, excellent analytical skills, and a strong background in the pharmaceutical industry. The company values work-life balance and offers competitive compensation and professional development opportunities.

Benefits

Competitive total compensation package

Professional development opportunities

Work-life balance

Pension

Life Assurance

Qualifications

• Minimum two years’ prior pharmaceutical industry experience in Pharmacovigilance or Medical/Clinical functions.
• Knowledge of worldwide PV-RMP regulations, with prior EU regulations experience.
• Ability to independently lead long- and short-term project timelines.

Responsibilities

• Serve as primary author for PV-RMPs, preparing according to regulatory requirements.
• Facilitate cross-functional review and approval of PV-RMPs.
• Collaborate with country organizations on PV-RMPs and related activities.

Skills

Analytical thinking

Interpersonal communication

Scientific writing

Education

Bachelor’s degree in nursing/biologic/medical/clinical field

Job description

A global healthcare company is seeking a PV Risk Management Specialist in Reading, England. The role involves developing Pharmacovigilance Risk Management Plans (PV-RMPs) and requires expertise in regulatory requirements, excellent analytical skills, and a strong background in the pharmaceutical industry. The company values work-life balance and offers competitive compensation and professional development opportunities.