Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID: 10683
As a memeber of the cross-functional Translational sub-team you will collaborate with a Translational Lead on the development and implementation of program-specific, integrated biomarker strategies from Ph1 to licensure, in alignment with clinical development objectives.
Your main responsibilities are:
* Contributing to the translation of preclinical results and approaches to clinical biomarker strategies supporting efficient clinical development of the assigned infectious disease assets through data-driven decision making and regulatory compliance
* Partnering with clinical, technical, and scientific colleagues to contribute to the overall biomarker strategy and assist in its execution
* Provides biomarker and translational contributions to the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications
* Contributes to the execution of the translational and biomarker strategy in the assigned development program(s)
What you have to offer:
* PhD, PharmD, or MD/PhD in Immunology, Biology, Biochemistry, Molecular Medicine, Virology or a related field with <4 years of relevant postdoctoral experience in academic, pharmaceutical, or biotechnology settings
* Minimum of 2-3 years of relevant working experience, preferably in industry settings
* Prior experience in infectious disease research or vaccine development
* Previous experience working with clinical samples and/or clinical biomarker assay development
* Experience with development and implementation of relevant biomarker and immunological assays, including ELISpot, ELISAs, flow cytometry, T cell-based assays, serological assays, etc.
* Demonstrated experience with innovative assay development and proven ability to effectively troubleshoot and solve complex problems. Experience in collaborating with external specialty laboratories is a plus
* Experience working in a multi-disciplinary team and ability to integrate cross-functional information
* Scientific accomplishments as evidenced by publications in peer reviewed journals
* Excellent, broad communication skills in various interpersonal settings
* Excellent organizational, communication skills, and attention to details
* Strong writing skills as demonstrated by authorship of peer-reviewed publications and contributions to regulatory communications (e.g., briefing documents, clinical trial protocols, marketing authorization applications)
* Eagerness to work in the dynamic environment of a fast-growing company
* Comfortable in working in a matrix environment (global/cross-functional)
Your Benefits:
It's our priority to support you:
* Your flexibility: flexible hours | vacation account
* Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
* Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
* Your health and lifestyle: Company bike
* Your mobility: Job ticket | Deutschlandticket
* Your life phases: Employer-funded pension | Childcare
Apply now - We look forward to your application!
Apply to our Mainz, Germany; London, United Kingdom; Munich, Germany location by sending us your documents via our online form. For any questions, contact our talent acquisition team on: + 49 (0) 6131-9084-1291 (Monday-Friday from 1 PM to 3 PM CET).
Job ID 10683 (please always specify if you have any questions)
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