Senior Pharmacovigilance Officer
placements24Easton (MA)
About the role
About the Role:
Our client seeks an experienced Senior Pharmacovigilance Officer to join their dedicated safety team, operating remotely to serve their operations in Welkom and beyond. This critical role focuses on the continuous monitoring and assessment of drug safety, ensuring the highest standards of patient protection throughout the product lifecycle. You will be responsible for managing adverse event data, conducting signal detection, and ensuring compliance with global pharmacovigilance regulations. This is an excellent opportunity to contribute to drug safety in the Free State from a remote setting, working with a leading pharmaceutical entity.
Key Responsibilities:
Oversee the collection, processing, and assessment of adverse event reports from various sources.
Conduct literature reviews and database searches to identify potential safety signals.
Prepare and submit regulatory safety reports (e.g., PSURs, DSURs) in accordance with regulatory timelines.
Develop and update pharmacovigilance procedures and training materials.
Collaborate with internal departments and external partners on safety-related matters.
Requirements:
Degree in Medicine, Pharmacy, Nursing, or other health-related sciences.
Significant experience (5+ years) in pharmacovigilance or drug safety.
In-depth knowledge of global pharmacovigilance regulations and reporting requirements.
Experience with safety databases and adverse event reporting systems.
Strong analytical skills and the ability to interpret complex safety data effectively.
Benefits:
Generous annual salary commensurate with experience, plus potential for bonuses.
Comprehensive health, dental, and vision insurance plans.
Retirement savings plan with employer contributions.
Extensive professional development opportunities, including specialized training.
Fully remote position offering significant work-life balance and flexibility.
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