PBPK Modeler (all genders) (permanent / full-time) at AbbVie
LAR, , Germany -
Full Time


Start Date

Immediate

Expiry Date

19 Sep, 25

Salary

0.0

Posted On

19 Jun, 25

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Data Analysis, Presentation Skills, Ddi, Pharmacokinetics, Biotransformation, Relationship Building, Dmpk

Industry

Information Technology/IT

Description

Unternehmensbeschreibung
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Stellenbeschreibung

THE JOB THAT HELPS YOU GET AHEAD IN LIFE. MOVING MOUNTAINS TOGETHER.

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 of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you
passionate about improving global health care? Do you want to contribute to improving patients’ quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!
Moving mountains together – as PBPK Modeler (all genders) (permanent / full-time)
The Quantitative, Translational and ADME Sciences (QTAS) team at AbbVie, Inc. is seeking a scientist in the Germany who can perform a role as Physiologically-Based Pharmacokinetics (PBPK) modeler to provide small molecule project support across multiple therapeutic areas. The successful candidate will be responsible for conducting static and mechanistic PBPK, human PK, and drug-drug interactions (DDI) projections using in vitro and in vivo ADME/PK data to support Discovery and Development project teams, enabling compound progression from discovery to early stages of clinical development. The position will require close collaboration with lab functions within QTAS, Discovery project teams and other R&D stakeholders in order to develop and execute QTAS strategies necessary to select and facilitate the advancement of optimized candidate molecules. In this exciting and dynamic role you will also be expected to evaluate new technologies and approaches to support the mechanistic and translational understanding of drug disposition and drug-drug interactions. The ideal candidate will have strong background in enzymology and DDI and hands-on experiences in PBPK modeling using a commercial software (e.g. Simcyp).

QUALIFICATIONS

  • Senior Scientist I: Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no (some) experience necessary
  • Senior Scientist II: Bachelor’s Degree or equivalent education and typically, 12 years of experience, Master’s Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience
  • Knowledge and experience in enzymology and DDI disciplines is required.
  • Experience with relevant modeling software, including Simcyp and Phoenix WinNonlin is strongly preferred.
  • Hands-on project experience in PBPK modeling and simulation through direct industry experience as well as knowledge of regulatory expectations regarding PBPK modeling is preferred
  • Experience in the field of DMPK with a general understanding of one or more disciplines within DMPK and knowledgeable in one or more of the following areas: in vitro ADME, pharmacokinetics, transporter, DDI, translational modeling, biotransformation, biomarker strategy
  • Demonstrated publication record; lead/senior author contributions a plus
  • Ability to influence, negotiate and communicate effectively with both internal and external stakeholders; ability to work well in a collaborative fast-paced team environment
  • Highly motivated, self-driven and results-oriented with excellent communication and presentation skills; capable of working both as team player and project driver
  • High degree of flexibility in adapting to different projects and people; excellent networking and relationship-building (both internal and external) skills
  • Passion for data analysis, solving technical problems and applying new technologies to further scientific goals
Responsibilities
  • Predict human PK and DDI profiles of small molecule drug candidates utilizing pre-clinical in vitro and in vivo ADME/PK data and static and mechanistic modeling tools
  • Support project teams across multiple therapeutic areas and interpret results through close partnership with QTAS representatives
  • Effectively communicate human PK/DDI prediction and PBPK modeling, QTAS strategy and knowledge to project teams, functional leaders, and other key stakeholders to ensure alignment and influence decisions
  • Demonstrate thorough understanding of drug metabolism, pharmacokinetics and bioanalysis (DMPK-BA) necessary for the characterization of small molecule drug candidates to support regulatory submissions
  • Stay current with latest developments in the field of human PK and DDI predictions including empirical (e.g. allomeric scaling) and more mechanistic models (e.g. PBPK)
    Qualifikationen
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