Biomapas
via Workable
Pharmacovigilance Associate Germany
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 28d ago
The date the source published, not the day we noticed it (2026-08-18). Last seen at its source 2h ago.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
Germany
The description states no restriction of its own. This is the source's own tag.
Carried by 1 source
-
workable employer's own board first seen 11d ago · last seen 2h ago
The listing
Join our global team as a Pharmacovigilance Associate in Germany.
Pharmacovigilance Associate performs routine PV tasks such as case intake, data entry, literature monitoring, and documentation management to support Local safety officers in the DACH region to maintain compliant PV operations, with further opportunity to be nominated as Local Safety Officer.
Position is remote/home-based in Germany.
All CVs must be submitted in the English language for consideration.
Responsibilities:
- Perform routine and foundational PV activities for assigned projects (e.g., case intake, data entry, coding, literature monitoring, distribution of safety information)
- Perform initial case intake and triage according to SOPs
- Enter and code cases in safety databases with supervision
- Assist in follow-up activities (requests, tracking, documenting)
- Prepare cases for quality control review and correct findings promptly
- End to end case processing steps under supervision
- Assist with administrative tasks related to PV systems, including preparing files, templates, and checklists
- Provide administrative support for audits/inspections
- Conduct weekly literature searches using predefined search strategies
- Document search results, identify potential safety cases, and escalate to upper level for assessment
- Preparation of data for Aggregate Safety Reports (PSURs/PBRERs), RMP/SMP sections, and risk minimization activities
Requirements
- University degree (or final year student) in Life Sciences or a related field
- Fluent written and verbal English and German language
- Foundational knowledge of pharmacovigilance principles and relevant regulatory frameworks
- Ability to perform routine PV tasks (case intake, data entry, literature review) accurately under supervision
- Good computer literacy and ability to learn safety databases and PV systems
- Good organizational skills and ability to manage a routine workload effectively
- Strong attention to detail and accuracy in documentation
Benefits
- Professional growth and career opportunities
- International team and environment
- Bonus based on annual performance
- Personal accident and business trip insurance
- Additional health insurance
- Remote/home-based position
- Rewarding referral policy
- Workplace establishment allowance
- Team building, global meetings, B active events