Pharmacovigilance Data Processor
hace 4 días
About the Role:
">- We are seeking a highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.
- In this critical role, you will be responsible for the accurate and timely intake, processing, and tracking of adverse event reports received from various sources.
- You will play a vital role in ensuring the safety of our products by diligently adhering to regulatory guidelines, internal Standard Operating Procedures (SOPs), and global best practices.
Responsibilities:
- Case Intake & Processing:
- Receive and process adverse event reports from various sources, including emails, faxes, phone calls, and databases.
- Conduct initial assessment and triage of adverse events to determine seriousness and reportability.
- Perform data entry and maintain accurate records in safety databases (e.g., Argus, APEX).
- Conduct follow-up with reporters to obtain missing information.
- Track and manage case processing timelines and ensure timely completion of all activities.
- Communicate effectively with internal stakeholders and external parties as needed.
- Collaborate with the Pharmacovigilance team to ensure efficient case processing and data management.
Requirements:
- Bachelor's degree in a life science field or equivalent experience.
- Fluent local language skills and excellent command of English language.
- 1+ years of experience in pharmacovigilance or a related field preferred.
- Strong attention to detail and accuracy.
- Excellent organizational and time-management skills.
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