Senior Pharmacovigilance Specialist — Drive Global Safety

Par Health; Hazelwood (MO); On-site; USD 80,000 - 100,000; Full time

Job summary

A healthcare organization in Hazelwood is looking for a Senior Pharmacovigilance Specialist to manage adverse event reports and ensure compliance with global regulations. The ideal candidate will have at least 5 years of clinical experience and thorough knowledge of safety reporting. This role necessitates strong communication skills and experience with adverse events management. The position involves independent work within a collaborative team environment and offers opportunities for professional development through occasional travel.

Qualifications

• Minimum of 5 years clinical experience in a relevant environment.
• Minimum of 3 years experience with post-marketing adverse events.
• Thorough knowledge of US and ICH safety reporting regulations.

Responsibilities

• Collect and document adverse event reports.
• Process and report serious adverse events.
• Review reports for quality and ensure regulatory compliance.

Skills

Knowledge of clinical areas

Reviewing and summarizing medical records

Excellent verbal and written communication

Computer applications (Word, Excel, PowerPoint)

Reporting and management of adverse event reports

Writing safety summaries

Education

Bachelor’s degree with healthcare certification

Job description

A healthcare organization in Hazelwood is looking for a Senior Pharmacovigilance Specialist to manage adverse event reports and ensure compliance with global regulations. The ideal candidate will have at least 5 years of clinical experience and thorough knowledge of safety reporting. This role necessitates strong communication skills and experience with adverse events management. The position involves independent work within a collaborative team environment and offers opportunities for professional development through occasional travel.