Luminary Group is currently seeking a dedicated and experienced Pharmacovigilance Specialist to join our client, a large pharma company. As a Pharmacovigilance Specialist, you will be responsible for monitoring and ensuring the safety of our pharmaceutical products in compliance with regulatory guidelines.

Responsibilities::

• Review and evaluate adverse event reports and other safety-related data for our pharmaceutical products.
• Conduct case processing activities, including data entry, coding, and narrative writing.
• Perform 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.
• Stay updated on current Pharmacovigilance regulations and guidelines.
• Assist in the development and implementation of Pharmacovigilance processes and procedures.
• Maintain compliance with company policies and standard operating procedures.
• Contribute to the continuous improvement of our Pharmacovigilance systems and activities.

Requirements:

• Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field.
• Minimum of 2 years of experience in Pharmacovigilance or a similar role.
• Strong knowledge of Pharmacovigilance practices and regulations.
• Experience with case processing activities, including data entry, coding, and narrative writing.
• Proficiency in using Pharmacovigilance databases and safety reporting systems.
• Attention to detail and accuracy in data entry and documentation.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work well both independently and in a team.
• Flexibility to work remotely and adhere to different time zones, if required.