Job Responsibilities:
Data Management:
- Enter and update information about medicinal products in the XeVMPD system in accordance with EU regulatory guidelines.
Quality Assurance:
- Ensure the accuracy and quality of data entered into the system.
- Regularly review and clean data to maintain its integrity.
Regulatory Compliance:
- Ensure compliance with all relevant regulatory guidelines related to XeVMPD.
- Keep up-to-date with changes in regulations and implement them in data management practices.
Collaboration:
- Work closely with other departments, such as Regulatory Affairs and Pharmacovigilance, to collect necessary information and ensure its correct entry into the system.
Reporting:
- Generate regular reports on data management activities and present findings to relevant stakeholders.
Training:
- Train other team members on XeVMPD data entry and management practices.
Problem Solving:
- Address and resolve any issues or discrepancies in the XeVMPD data promptly.
Requirements:
- Degree in Pharmacy, Life Sciences, or a related field.
- Experience in Pharmacovigilance or Regulatory Affairs.
- Strong attention to detail.
- Knowledge of EU regulations related to drug safety.
- Proficiency in data management systems.
