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# Data Officer

- **Company:** Groupe ProductLife
- **Location:** Wettolsheim, France (Remote available)
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Databases, Microsoft Office, Microsoft PowerPoint, Data Management
- **Published:** August 4, 2026
- **Apply:** https://candidateportal.ceipal.com/job-details/lobPDNt1PVwnZ-wQhBwLD5lPWQ3i55FBkCkQ37bGIfA

## About the Role

* Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Biology, or a related scientific discipline., * Minimum 2 years of experience in pharmacovigilance data entry within a post-marketing environment.
 * Experience handling and processing ICSRs.
 * Proven experience with XEVMPD activities., * Excellent written and verbal communication skills in English.
 * Additional languages are considered an asset., * Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).
 * Strong attention to detail and data accuracy.
 * Excellent organizational and time-management skills.
 * Process-oriented mindset.
 * Ability to work effectively in a team environment.
 * Flexibility and adaptability in a fast-paced setting., * Experience working with pharmacovigilance databases.
 * Knowledge of regulatory pharmacovigilance requirements.
 * Previous exposure to safety database management systems.
 * Additional experience with XEVMPD maintenance and data management.
 * Database experience is preferred; training will be provided where needed., * Attention to Detail
 * Customer Focus
 * Accountability
 * Teamwork and Collaboration
 * Communication Skills
 * Problem Solving
 * Planning and Organization
 * Quality Orientation

## Description

* Perform triage, review, and data entry of pharmacovigilance cases.
 * Process and maintain Individual Case Safety Reports (ICSRs) in accordance with applicable regulations and internal procedures.
 * Support the submission of ICSRs to health authorities, clients, and partners.
 * Manage and monitor assigned pharmacovigilance mailboxes.
 * Follow up directly with consumers, patients, healthcare professionals, and other stakeholders to obtain missing safety information when required.
 * Perform XEVMPD (Extended EudraVigilance Medicinal Product Dictionary) related activities.
 * Ensure data accuracy, completeness, and consistency across safety databases.
 * Maintain compliance with quality standards, SOPs, and regulatory requirements.
 * Collaborate effectively with cross-functional teams and stakeholders.
 * Support continuous improvement initiatives and operational excellence activitie


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