Senior Principal Toxicologist (all genders) - (unlimited / fulltime)

☞ AbbVie

Vue: 178

Jour de mise à jour: 22-10-2024

Localisation: Ludwigshafen am Rhein Rhineland-Palatinate

Catégorie: R & D IT - Logiciel

Industrie: Biotechnology Research Pharmaceutical Manufacturing

Niveau: Mid-Senior level

Type d’emploi: Full-time

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le contenu du travail

Welcome to AbbVie!As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity to work closely with us to address the health challenges of tomorrow. Do you have a passion for improving health care around the world and for using your expertise to improve patients’ quality of life? In a challenging work environment that allows you to broaden and develop your own skills? You’ve found the right place!

The Preclinical Safety department in Ludwigshafen am Rhein is looking for aSenior Principal Toxicologist (all genders) - (unlimited / fulltime) who supports the development of new therapies by setting preclinical safety strategies as well as performing preclinical safety studies in house, especially for neurological diseases. We are a diverse team and work closely with global project teams as well as with our headquarter in Chicago. Together, we overcome obstacles and advance science.

The Senior Principal Toxicologist will:

  • Support all therapeutic areas by leading a team of study directors. In this role, the candidate will demonstrate strong proactive scientific leadership by advising, sharing knowledge, and mentoring to guide conduct and reporting of non-GLP in vivo toxicology studies. In close interactions with other teams within PCS, the Senior Principal Toxicologist will enable constant process improvement and scientific development
  • In addition, the applicant is expected to support our portfolio with a special emphasis on neuroscience projects as a project team member. In this role, the candidate will
  • Provide scientific and technical leadership for the selection and development of various therapeutic modalities (e.g., small molecules, biologics, gene therapies)
  • Contribute to the development of a scientific and regulatory strategy for assigned projects
  • Assess and review of non-clinical and clinical protocols, reports and scientific documents generated for regulatory purposes and
  • Represent PCS in in global project teams
  • Prepare and review nonclinical submission documents and interact with regulatory agencies in multiple regions
  • Advance scientific expertise within the function by contributing own expert opinion, peer-reviewing documents and by demonstrating superior scientific leadership

Qualifications of the Senior Principal Toxicologist:

  • Holds a Ph.D. (or equivalent) in toxicology or related field and at least 10 years’ experience within the Pharmaceutical Toxicology fiel
  • Toxicology (or related field) board certification preferred
  • Experience as a toxicology study director and monitor
  • In depth knowledge of regulatory preclinical aspects of drug development of therapeutic proteins and small molecules
  • Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators
  • Previous supervisory experience preferred
  • Experience in process improvement

We offer you:

  • A passionate team of highly committed colleagues
  • We are happy to support your relocation and accompany your on-boarding process
  • We provide our employees with high flexibility to tailor their daily work to their individual needs, including flexible work models, multiple benefits, and comprehensive health and sports programs
  • Attractive compensation and company benefits, including our excellent occupational health management system, which is one of the best in Germany as well as a wide range of career paths and opportunities for further development

At AbbVie, your individual contributions count – help us achieve more together. Be a part of it and grow with us – go above and beyond!

Sounds like the perfect career opportunity for you? We look forward to receiving your application. All you need is a complete CV – anything else will be discussed in person, where possible, if general suitability is determined.

Have questions? Email us at TalentAcquisition.de@abbvie.com – we look forward to hearing from you!

At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity and affirmative action employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. If you would like to view a copy of the company’s affirmative action plan or policy statement, please email CorpJat_ABV@abbvie.com.
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Date limite: 06-12-2024

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