Biomapas
via Workable
Pharmacovigilance Specialist
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 2d 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 6d ago
The date the source published, not the day we noticed it (2026-09-09). Last seen at its source 1h 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?
Turkey
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 5d ago · last seen 1h ago
The listing
Delta PV, a leading pharmacovigilance service provider headquartered in Istanbul, Türkiye, has been part of the Biomapas group since 1 August 2025. As such, this vacancy is advertised on behalf of Delta PV within the Biomapas organization.
Pharmacovigilance Specialist is responsible for operational delivery for assigned tasks on the project level. Pharmacovigilance Specialist can act as the Primary or Secondary Project Responsible for the project assigned. Pharmacovigilance Specialist is communicating to Pharmacovigilance Team Leader/ Pharmacovigilance Manager about potential risk related to operational delivery, quality, client relationship and company reputation, as well as ad hoc project tasks and project requirements. Pharmacovigilance Specialist can be engaged in company’s procedures review and update.
Responsibilities
- Performing tasks based on weekly work planning meetings.
- Performing tasks in cooperation with the Pharmacovigilance Managers and Team Leaders according to a specified plan.
- Supporting weekly/monthly local and global literature screening.
- Translation of adverse events and quality complaints from Turkish to English.
- Entering cases into database system and generating their formal reports.
- Supporting follow-up of safety alerts.
- Ensuring that reconciliation process is in place and performed regularly with clients.
- Ensuring continuity of PV activities in the absence of a Pharmacovigilance Specialist.
- Following the principles of data integrity, confidentiality and personal data protection, as applicable.
- Continuously developing his/her professional and personal skills and participating in pharmacovigilance relevant trainings.
Requirements
- A Pharmacy degree (Mandatory).
- Excellent written and oral communication skills in English and Turkish (MANDATORY).
- At least 1 year PV experience.
- Experience in pharmaceutical companies is an advantage.
- Exposure to healthcare/life-sciences industry is an advantage.
Benefits
- Professional growth and career opportunities
- International team and environment
- Health & Life Insurance
- Monthly Food Allowance
- Monthly Transportation Fee
- Remote Work