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Pharmacovigilance and Medical Research Associate
Purpose of the Position:
The purpose of this position is to carry out post-marketing safety studies of the seasonal influenza vaccine in compliance with regulatory requirements. In addition, the role involves participation in pharmacovigilance and clinical research tasks
Main Responsibilities:
- Primary responsibility is the planning, organization, and full execution of the safety study, including monitoring of the study and maintaining continuous communication with the investigators.
- Participation in the management of adverse events and spontaneous suspected side effect reports received in the pharmacovigilance system.
- Participation in tasks related to the conduct of clinical trials.
- Contribution to the preparation of pharmacovigilance and clinical study reports, and where applicable, preparation of relevant parts of registration documentation.
Requirements:
- Degree in natural sciences; medical, dental, pharmaceutical, or biology degree is an advantage.
- Experience in pharmacovigilance and/or clinical trial coordination/monitoring; knowledge of both fields is an advantage.
- Professional proficiency in English.
- User-level computer skills.
- Driving license and driving experience.
Work Location: Budaörs, with partial possibility of remote work. Occasional travel depending on tasks: Pest county, Debrecen.
Working Hours: Full-time
IT Administrator L1
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