Pharmacovigilance Expert/Associate - Full Time Remote

Overview

Luminary Group is seeking a motivated and experienced Pharmacovigilance Expert/Associate to join our client, a large pharmaceutical company on a full-time remote basis. As a Pharmacovigilance Expert/Associate, you will play a vital role in ensuring the safety and efficacy of our client's pharmaceutical products.

In Short

• Review and evaluate adverse event reports and other safety-related information for our client's products.
• Perform case processing activities, including data entry, coding, narrative writing, and quality checks.
• Conduct signal detection activities and contribute to the preparation of signal evaluation reports.
• Collaborate with cross-functional teams to ensure timely and accurate reporting of adverse events to regulatory authorities.
• Assist in the development and implementation of Pharmacovigilance processes and procedures.
• Maintain knowledge of current regulatory requirements and guidelines related to Pharmacovigilance.
• Ensure compliance with company policies and standard operating procedures.
• Contribute to the continuous improvement of Pharmacovigilance activities and systems.

Requirements

• Experience in Pharmacovigilance or related field.
• Strong analytical and problem-solving skills.
• Excellent communication and collaboration abilities.
• Knowledge of regulatory requirements in Pharmacovigilance.
• Attention to detail and commitment to quality.

Benefits

• Work remotely from anywhere in China.
• Opportunity to work with a large pharmaceutical company.
• Professional development opportunities.
• Collaborative work environment.