PLG is looking for a dedicated Data Officer to join our Pharmacovigilance (PV) team to manage, maintain, and ensure the accuracy and quality of safety data. The role involves overseeing the secure handling, entry, and reporting of data on adverse events, ensuring compliance with regulatory standards across various healthcare products.

Group 10
Responsibilities

1. Data Management and Entry

  • Accurately input safety data (e.g., adverse events, reactions) into PV databases.
  • Maintain up-to-date and comprehensive data records for medicinal products and devices.

2. Data Quality Control

  • Conduct regular quality checks to ensure the integrity and accuracy of all safety data.
  • Identify and resolve any inconsistencies or missing data.

3. Data Security and Compliance

  • Ensure all data handling complies with Good Pharmacovigilance Practices (GVP) and regulatory guidelines.
  • Maintain strict confidentiality and security protocols for sensitive safety data.

4. Reporting and Documentation

  • Assist in generating reports for regulatory submissions, audits, and internal reviews.
  • Ensure all documentation meets regulatory requirements and company standards.

5. Collaboration

  • Work closely with PV specialists, case handlers, and regulatory teams to provide accurate safety data.
  • Support audits and inspections by retrieving and preparing data reports.

Group 12
Experience

  • Education: Degree in Life Sciences, Pharmacy, or related field.
  • Experience: Previous experience in data entry, management, or pharmacovigilance (preferably 1-2 years).
  • Technical Skills: Proficiency in Microsoft Office and familiarity with PV databases (e.g., Argus, ArisG).
  • Knowledge: Understanding of GVP and regulatory standards related to pharmacovigilance.

Data Officer - 352

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