AbbVie

Project Data Manager / Associate Scientist II (all genders) (full- or parttime, temporary for 1[...]

Stellenbeschreibung:

Project Data Manager / Associate Scientist II (all genders) (full- or parttime, temporary for 18 months)

Workday Global Grade: 10

Responsibilities

  • Support cross‑functional laboratory sample and data operations in all stages of AbbVie clinical trials and in compliance with GCP/GLP requirements
  • Initiate, coordinate and revise documents for setting up projects/services with vendors, for example on the external storage of clinical trial samples
  • Support sample data curation, intake, reconciliation and transfer using bioanalytical LIMS and ELN software
  • Support internal and external sample storage management including inventorying stores, reviewing retention periods, and coordinating relocation and disposal
  • Collaborate with global teams to support cross‑functional processes and data exchange
  • Contribute to the development and testing of IT systems or process enhancements
  • Ensure compliance with regulatory requirements and SOPs as well as adherence to flexible project timelines

Qualifications

  • Completed vocational training, successful completion of additional training in life sciences, clinical research, data management, or a comparable discipline; the vocational training may be replaced by equivalent knowledge acquired through relevant professional experience. A bachelor’s degree or equivalent with at least 3 years of professional experience, or a master’s degree or equivalent (without professional experience) is preferred.
  • Previous experience that demonstrates the knowledge, skills, and abilities to perform the job (comparable to 1+ years).
  • Proficient in MS Excel, MS Teams and other MS Office applications.
  • Demonstrated experience and/or knowledge in specialized data‑management software, for example Laboratory Information Management Systems (LIMS) or comparable databases.
  • Demonstrated experience in clinical trial operations (logistics, records, data) or other GLP/GCP/GMP‑regulated operations is a plus.
  • Ability to work in a collaborative environment with process and SOP compliance and attention to detail.
  • Strong English language skills (oral and written).
  • Basic German language skills are an advantage.
  • Flexible work hours (to partly cover USA CT time zones).

Benefits

  • Work in a diverse environment where you can have a real impact
  • Open corporate culture
  • Attractive salary
  • Intensive onboarding process with a mentor at your side
  • Flexible work models for a healthy work‑life balance
  • Corporate health management with comprehensive health and exercise programs
  • Company social benefits
  • Wide range of career opportunities in an international organization
  • Top‑tier development opportunities
  • Strong international network

The position is fixed term until 30 November 2027.

For part‑time employment, the minimum scope is 80%.

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Stelleninformationen

  • Veröffentlichungsdatum:

    10 Mai 2026
  • Standort:

    Ludwigshafen am Rhein

    Einsatzort:

    Ludwigshafen
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

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