Pharmacovigilance Specialist (Submissions specialist) Taiwan

Biomapas

Taiwan Remote permanent

Posted: February 13, 2026

Quick Summary

The Pharmacovigilance Specialist (Submissions specialist) in Taiwan is responsible for managing regulatory submission activities, reviewing submission data packages, and ensuring compliance with safety reporting requirements. The role involves coordinating submissions, tracking status, and documenting and archiving data. This is a remote position, with a focus on Taiwan and the US.

Job Description

The Submission Specialist is responsible for the timely and accurate management of regulatory submission activities at the project level. The role includes reviewing submission data packages for completeness and regulatory compliance, supporting preparation activities, and ensuring adherence to applicable safety reporting requirements.

The Specialist manages submission workflows, coordinates timely submissions, tracks submission status, collects acknowledgements, and ensures proper documentation and archiving in line with project and country-specific regulations. Regular communication with clients regarding submission status is also required.

Responsibilities:

• Submission data package review for completeness, accuracy and regulatory reportability

• Assisting the client in and/ or submission data package preparation
• Maintaining and/ or applying of safety reporting regulatory intelligence
• Submission process workflow management for expeditive (foreign and local) and periodic reports (PSUR, DSUR).
• Performing/ coordinating timely submission of submission data package
• Acknowledgement of receipt/ proof of submission collection
• Tracking of safety submissions
• Documentation filing and archiving according to project and country specific requirements
• Notification on submission status to the client/ responsible party
• Communication with TFDA as applicable
• Performing trainings on time

Requirements:
• Bachelor’s degree in Life Sciences field
• Minimum 1 year of experience in pharmacovigilance or safety case processing within the pharmaceutical or CRO industry in Taiwan
• Fluency in Mandarin Chinese (Simplified Chinese) and English languages (Mandatory)
• Experience with case submissions to local Health authorities (Mandatory)
• Hands-on experience with Argus Safety, Veeva Vault or similar safety databases is preferred
• Strong proficiency in MS Office applications
• Ability to work independently while managing multiple cases and deadlines
• Candidates needs to be based in Taiwan

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