Luminary Group
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.
Responsibilities:
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
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.
Ability to work independently and prioritize tasks effectively.
Excellent attention to detail and accuracy in data entry and documentation.
Strong analytical and problem-solving skills.
Good interpersonal and communication skills, with the ability to effectively collaborate with cross-functional teams.
Flexibility to work remotely and adhere to different time zones, if required.
Luminary Group
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