For our Pharmacology/Toxicology department we are looking for a

Scientist - Pharmacology, Cardiovascular & Metabolic (m/f/x) – R-213070

(Fulltime / Permanent/ Tarif)

Role

As a member of the In Vivo Pharmacology (IVP) Unit, the Scientist - Pharmacology (CV&M) is responsible for planning, coordinating, executing, and reporting of in vivo and in vitro pharmacology studies of regulatory relevance within the therapeutic area of Cardiovascular and Metabolic (CV&M) diseases. The activities will furthermore involve setting up animal models of disease, supervising PhD students (if required) and laboratory technicians (task-based) and working in matrix teams across different functional areas. The Scientist -Pharmacology, CV&M will act as pharmacology representative in global cross-functional research and development teams and will be responsible for authoring and reviewing the non-clinical pharmacology sections of national and international regulatory submission documents.

Main Responsibilities and Accountabilities:

• Plan, initiate and perform pharmacology studies, including proof of efficacy, dose range and time course studies, within the CV&M Therapeutic Area
• Coordinate and report preclinical pharmacological studies (in vivo, ex vivo and in vitro) conducted internally or in collaboration with external sites at the highest levels of scientific integrity; thereby supporting characterization of drug candidates
• Establishment of new animal models of disease (incl. writing of required ethics applications) and support the identification and generation of biomarker data.
• Actively collaborate with and contribute to global, cross-continental project teams; and parties within and outside of own job function
• Close interaction/alignment with other internal stakeholders and partners to develop and deliver on the non-clinical pharmacology strategy and objectives within the CV&M Therapeutic Area
• Support the preparation of national and international regulatory submissions Provide scientific expertise and guidance in the application of relevant technology platform to research and product development activities.
• Ensure high quality application of existing and novel technology platforms in order to support designated project objectives

Experience in the following areas is an advantage:

• Experience with regulatory processes in the pharmaceutical industry
• Experience with echocardiography and telemetry is a plus
• Previous completion of a relevant FELASA course is desired

Qualifications & Experience:

• A University Degree in a relevant field of Science (e.g. Bachelor of Science in biology, cardiovascular physiology or pharmacology)
• Hands-on experience in relevant in vivo models and laboratory techniques.
• English Level 2, fluent in German
• 4-5 years of relevant experience

Marburg, 05.09.2023

CSL Behring Innovation GmbH

Human Resources

R-213070

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CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

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