Remote Pharmacovigilance Specialist — Safeguarding Drug Safety

Placements24; Waukee (IA); Hybrid; USD 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Competitive salary

Medical aid

Retirement plan

Flexible remote hours

Professional development

Supportive team

Zusammenfassung

Placements24 is seeking a proactive Remote Pharmacovigilance Specialist to join their safety team, supporting pharmaceutical operations from anywhere within the United States. You will monitor, evaluate, and report adverse events in line with global PV regulations.

The role requires a Bachelor's in a health field and at least 3 years in pharmacovigilance, with strong MedDRA and data-entry skills, and the ability to liaise with clinicians and regulators.

Qualifikationen

• Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related field.
• Minimum 3 years of pharmacovigilance or drug safety experience.
• Strong knowledge of global PV regulations (ICH E2B, GVP).
• Experience with MedDRA coding and safety databases.
• Excellent written and verbal communication for regulatory reporting.

Aufgaben

• Collect, assess, and document adverse event reports from multiple sources.
• Perform case processing, data entry, and causality/seriousness assessment.
• Prepare and submit PSURs and DSURs as required.
• Conduct literature searches for safety signals.
• Liaise with healthcare professionals and regulators on safety matters.
• Help develop PV procedures and training materials.

Kenntnisse

Pharmacovigilance

MedDRA coding

ICH E2B/GVP

Data entry

Regulatory liaison

Safety databases

Analytical skills

Attention to detail

Effective communication

Ausbildung

Bachelor's degree in Pharmacy/Life Sciences

Tools

MedDRA coding tools

Safety database systems

Jobbeschreibung

Placements24 is seeking a proactive Remote Pharmacovigilance Specialist to join their safety team, supporting pharmaceutical operations from anywhere within the United States. You will monitor, evaluate, and report adverse events in line with global PV regulations.

The role requires a Bachelor's in a health field and at least 3 years in pharmacovigilance, with strong MedDRA and data-entry skills, and the ability to liaise with clinicians and regulators.