Senior toxicologist
- Marburg, Universitätsstadt
stellenbeschreibung
Job Description With operations in 35+ nations and ~ 22, 000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein bio-thera-peutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a trans-continental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! For our Pharmacology & Toxicology department we are looking for a Senior Toxicologist (m/f/d) (fulltime / permanent / non-tariff) - The Regulatory Toxicologist provides cross-functional leadership and in-depth scientific knowledge for compiling high-quality, strategically aligned nonclinical submission documents across all projects. - In addition he / she will apply state-of-the-art scientific methods and assessment of data to compile interpretation and conclusions of non-clinical study results and appropriate presentation to management and health authorities. - He or she is also responsible for the messaging strategy across a pro-gram of work, for the pro-vision of strategic input into the development of nonclinical development plans and submission plans, and for analyzing proposed plans, pro-grams, individual studies and related docu-ments for their ability to deliver the information required by the target audience (i. e., regulatory authority) in a compelling fashion with accuracy and consistency. - In addition, the jobholder will support Pharma-cology and Toxicology as project toxicologist and in compiling publications and toxicology assess-ments. - This role has global responsibilities, including participation in global teams and interaction with regulatory agencies in multiple regions. This role reports to the Director Toxicology. - PhD or Master in relevant scientific discipline (eG. Preferred
:toxicology, pharmacology, depending on experience:
other relevant natural science) - minimum of five-year experience in pharma-ceu-tical industry - minimum of three-year experience in toxicology - experience in compiling nonclinical regulatory sub-mission documents (at least 5 global submissions incl. inds completed) - experience in development of biologics - excellent english skills (verbal and written) or english native speaker with good german skills - very good knowledge of documents formatting (ms word, pdf) - strong negotiation skills and ability to identify and engage internal and external expertise as needed>
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