Job overview
as a pharmacovigilance specialist, you will be responsible for processing safety data according to applicable regulations and guidelines. Your key tasks will include database entry, coding adverse events, and writing narratives.
* process safety data in accordance with regulations and guidelines
* database entry and initial status updates of incoming events
* coding ae and products, writing narratives, literature-related activities, quality review
you will contribute knowledge and expertise to assigned deliverables in the field of safety publishing, risk management, and medical information. Ensuring compliance to project processes is crucial.
responsibilities
* meet quality, productivity, and delivery standards per project requirements
* liaise with stakeholders to facilitate expedited reporting
* contribute to a team environment, provide training and mentoring
requirements
* bachelor's degree in life science or related field
* at least 3 years' experience in pharmacovigilance or related area
* advanced experience with oracle argus safety
in this role, you will play a vital part in ensuring patient safety through effective pharmacovigilance practices. If you have strong analytical skills and excellent communication abilities, we encourage you to apply for this exciting opportunity.