Pharmacovigilance Officer

Placements24; United States; Híbrido; USD 36 000 - 54 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Hybrid work model

Competitive salary and incentives

Comprehensive health and wellness

Resumo da oferta

Placements24 is seeking a dedicated Pharmacovigilance Officer for a hybrid role based near Randburg. You will collect and assess adverse event reports, ensure regulatory reporting, and support SOPs and training within a safety-focused team.

The role requires a degree in a healthcare field and proven PV experience, with strong knowledge of global drug safety regulations and excellent communication skills. Hybrid work model and development opportunities are offered.

Qualificações

• Bachelor's degree or equivalent in a healthcare field as listed.
• Proven pharmacovigilance or drug safety experience is required.
• Thorough knowledge of global drug safety regulations (e.g., GVP).
• Strong attention to detail, analytical mindset and ability to multitask.
• Excellent written and verbal communication skills.

Responsabilidades

• Collect, process and assess adverse event reports per regulatory requirements.
• Ensure timely and accurate reporting of safety information to authorities.
• Develop and maintain pharmacovigilance SOPs and training materials.
• Conduct literature reviews for safety signal detection and risk management.
• Collaborate with cross‑functional teams to ensure global compliance.

Conhecimentos

Pharmacovigilance

GVP knowledge

Attention to detail

Analytical skills

Communication skills

Multitasking

Formação académica

Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related healthcare field

Descrição da oferta de emprego

About the Role

Our client is seeking a dedicated and vigilant Pharmacovigilance Officer to join their safety monitoring team based in Randburg . This hybrid role is crucial for ensuring the safety of patients by collecting, assessing, and reporting adverse events associated with pharmaceutical products. You will work collaboratively with regulatory affairs, medical affairs, and clinical operations teams to maintain a robust safety surveillance system. The ideal candidate possesses a strong understanding of regulatory requirements for pharmacovigilance and a commitment to patient safety and data integrity.

Key Responsibilities

• Collect, process, and assess adverse event reports from various sources according to regulatory requirements and company procedures.
• Ensure timely and accurate reporting of safety information to regulatory authorities and other stakeholders.
• Participate in the development and maintenance of pharmacovigilance SOPs and training materials.
• Conduct literature reviews for safety signal detection and contribute to risk management plans.
• Collaborate with cross‑functional teams to ensure compliance with global pharmacovigilance regulations.

Requirements

• Bachelor's degree in Pharmacy, Nursing, Life Sciences, or a related healthcare field.
• Proven experience in pharmacovigilance or drug safety.
• Thorough knowledge of global drug safety regulations and reporting requirements (e.g., GVP).
• Excellent attention to detail, analytical skills, and ability to manage multiple tasks.
• Strong written and verbal communication skills.

Benefits

• Competitive salary and performance-related incentives.
• Hybrid work model providing flexibility between office and remote work.
• Comprehensive health and wellness benefits.
• Ongoing training and professional development opportunities in pharmacovigilance.
• A crucial role in ensuring the safety and well‑being of patients using pharmaceutical products.