Remote Pharmacovigilance Officer: Patient Safety Advocate

Placements24; Southampton; Remote; GBP 40,000 - 65,000; Full time

Benefits offered by this job

Flexible remote work

Job summary

Placements24 seeks a Pharmacovigilance Officer to join a respected pharmaceutical organization. This fully remote role focuses on monitoring, processing, and reporting adverse events, ensuring global safety compliance.

You will manage safety data, contribute to PSURs, liaise with regulators, and maintain pharmacovigilance procedures while working independently from a remote environment. 3+ years in PV and strong analytical skills are expected.

Qualifications

• Bachelor's or master's degree in Pharmacy, Nursing, Medicine, or life science field.
• 3+ years in pharmacovigilance, drug safety, or clinical safety.
• Strong knowledge of global pharmacovigilance regulations and guidelines (ICH-GCP, CIOMS).
• Experience with adverse event case processing and reporting.

Responsibilities

• Process, evaluate, and report AE/ADR cases within regulatory timelines.
• Ensure safety data accuracy and quality.
• Perform literature searches for safety signals.
• Assist PSURs and other regulatory safety documents.
• Develop and maintain PV procedures and SOPs.
• Liaise with regulators, healthcare professionals, and internal teams.
• Attend safety review meetings and support risk management planning.
• Identify potential safety signals and assess them.
• Ensure compliance with local and international PV regulations.
• Maintain safety databases and records.

Skills

Analytical skills

Attention to detail

Verbal communication

Written communication

Remote work self-management

Education

Bachelor's or Master's degree in Pharmacy/Nursing/Medicine or life sciences

Tools

Pharmacovigilance software

Job description

Placements24 seeks a Pharmacovigilance Officer to join a respected pharmaceutical organization. This fully remote role focuses on monitoring, processing, and reporting adverse events, ensuring global safety compliance.

You will manage safety data, contribute to PSURs, liaise with regulators, and maintain pharmacovigilance procedures while working independently from a remote environment. 3+ years in PV and strong analytical skills are expected.