Clinical Safety Experts
7 dni temu
We are seeking a seasoned Pharmacovigilance Scientist to join our team at TN Poland. The successful candidate will be responsible for leading the safety component of global regulatory submissions, providing in-depth medical/scientific expertise in the safety evaluation and risk management of key assets.
Main Responsibilities:- Leads pharmacovigilance and risk management planning and develops strategy for approach to evaluation of issues in the clinical matrix.
- Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate.
- Makes recommendations for the further characterization, management, and communication of safety risks.
TN Poland is a leading biopharmaceutical company dedicated to unifying science, technology, and talent to get ahead of disease together. We have a strong commitment to innovation, quality, and patient-centricity, and we are looking for individuals who share these values.
Requirements:- Relevant degree qualification in life science discipline or relevant experience (Dentists and Veterinarians are also accepted).
- Advanced experience in the pharmaceutical or biotech industry working in pharmacovigilance, drug safety, medical affairs, or a related field.
- Significant pharmacovigilance experience relating to safety evaluation and risk management, encompassing both clinical development and post-marketing activities.
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