Job Description

Luminary Group is excited to announce an opportunity for a skilled Pharmacovigilance Specialist to join a top pharmaceutical company. This is a fantastic chance to contribute to patient safety by managing and reporting safety data and ensuring compliance with regulatory requirements.

Responsibilities:

• Monitor and analyze adverse events and safety data for various drug products.

• Conduct thorough case reviews, documentation, and safety assessments.

• Prepare and submit safety reports to health authorities in compliance with relevant regulations.

• Participate in safety signal management and contribute to risk management plans.

• Work collaboratively with internal teams to facilitate timely and accurate reporting of safety information.

• Stay informed on current Pharmacovigilance regulations and industry standards.

• Assist in the development and refinement of Pharmacovigilance processes.

• Engage in training and mentoring roles for junior staff members.

Requirements

• Bachelor's or higher degree in Pharmacy, Life Sciences, or a relevant field.
• At least 3 years of experience in Pharmacovigilance or related areas within the pharmaceutical industry.
• In-depth understanding of Pharmacovigilance regulations and guidelines.
• Experience with case processing, including data entry, coding, and writing comprehensive narratives.
• Proficient in using industry-standard Pharmacovigilance databases and tools.
• Meticulous attention to detail with a focus on data integrity.
• Strong analytical skills to evaluate safety data effectively.
• Excellent written and verbal communication skills.
• Ability to thrive in a fast-paced environment and manage multiple priorities.
• Willingness to work as part of a dynamic team while also demonstrating independence.

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