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**Role Overview:**
- Support a new pharmacovigilance program for a leading pharmaceutical company.
- Translate PBRERs and related safety documents with strict 24-hour TAT.
**Responsibilities:**
- Perform MTPE of PBRERs and ensure regulator-ready quality.
- Manage multiple projects simultaneously with strict deadlines.
**Requirements:**
- Minimum 2 years of experience in pharmacovigilance or clinical translation.
- Based in US or able to cover US time zones; commit 5+ hours daily.
**Tools and Process:**
- Use XTM CAT tool; client-provided license and onboarding.
- Complete an unpaid pharmacovigilance test as part of onboarding.
Welo Life Sciences
Welo Life Sciences is a specialized language and technology partner for pharmaceutical, CRO, and medical device companies, providing regulator-ready translation and localization solutions. They serve global markets with ISO-certified processes and technology-enabled workflows, supporting clinical trials and regulatory compliance.