Clinical Safety Specialist

vor 2 Wochen


Wien, Wien, Österreich Octapharma Vollzeit
Key Responsibilities

As a Clinical Safety Specialist at Octapharma, you will be responsible for supporting the Clinical Safety Project Lead in managing and executing safety-related activities within clinical trials. This includes coordinating and standardizing safety management tasks and reporting activities at different sites, as well as preparing study-specific safety management plans.

Your Profile

We are looking for a highly organized and analytical individual with a strong background in clinical safety or a related field. You should have a university degree in natural sciences or clinical sciences and experience in clinical research. Knowledge of safety regulations and reporting requirements is essential, as is the ability to work effectively in a team and communicate with various stakeholders.

What We Offer

As a valued member of our team, you will enjoy a wide range of tasks in an international setting, with flexibility and personal responsibility. You will also benefit from a reliable employer with generous employee benefits and a salary customary in the market. Our company culture is characterized by a family-owned enterprise with benefits such as a staff restaurant, extraordinary staff events, and more.

About Octapharma

Octapharma is a leading human protein manufacturer with a global presence. We develop and produce human proteins from human plasma and human cell lines, employing nearly 12,000 people worldwide. Our products are used to treat patients in 118 countries across three therapeutic areas: Immunotherapy, Haematology, and Critical Care.



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