Job description:
The Pharmacovigilance Intern supports the Pharmacovigilance team by assisting with assigned
operational activities under supervision, in compliance with applicable SOPs and project
requirements. The role contributes to case intake, data entry, documentation, tracking, and basic
safety database activities, while promptly escalating issues or uncertainties to the supervising
Pharmacovigilance Specialist, Team Leader or Regional PV/MI Lead. The intern does not perform
independent analysis, quality control, or approval activities.
Key Responsibilities:
- Provide operational and administrative support to the Pharmacovigilance team under supervision,
- Perform assigned tasks in compliance with SOPs, work instructions, and project requirements,
- Support case intake, registration, tracking, and documentation activities,
- Assist with data entry and basic case processing activities in safety databases under supervision,
- Support local literature screening and maintain related trackers and records,
- Assist with preparation, filing, archiving, and organization of PV documentation and reports,
- Support signal detection and aggregate reporting activities through data compilation and preliminary checks,
- Complete required PV trainings and escalate issues or deviations to the responsible PV personnel.
Requirements
- Undergraduate student or Bachelor’s Degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Preferably internship or entry-level experience in Pharmacovigilance, Safety, Pharmaceutical, or CRO industry.
- Strong verbal and written communication skills in English and/or local language,
- Good knowledge of MS Office applications,
- Based in Türkiye
Benefits
- Professional growth and career opportunities
- International team and environment
- Monthly Food Allowance
- Remote Work
Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success. We keep our promises. Always. Social media privacy policy: bit.ly/privacy-biomapas
Key team members
Tomaz Trcek
Martijn van de Leur
Valdis Tocs
Inga Garliauskiene
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