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Principal Research Scientist

2 months ago


New Hyde Park, New York, United States Cerba Research Nederland Full time
About the Role

Cerba Research Nederland is seeking a highly skilled and experienced Principal Scientist to join our team. As a key scientific position within our organization, you will play a crucial role in the development of new assays and ensuring the production of high-quality data for global clinical trials.

Key Responsibilities
  • Scientific Consultation
    • Interact with clients to provide expert consultation on scientific matters.
    • Support the sales team as an expert consultant for clients during client visits and/or via teleconferences.
    • Provide updates to clients during assay development and validation, and as needed for clinical data.
  • Point of Contact
    • Provide internal support for the implementation of assays by providing input to other divisions within Cerba Research.
    • Provide support for the implementation of assays in subcontractor laboratories.
    • Write validation plans, validation reports, working instructions, and SOPs.
    • Discuss validation data with clients as needed.
  • Internal Expertise
    • Maintain personal scientific and technical expertise in selected areas.
    • Maintain personal knowledge on therapeutic areas of assays validated at Cerba Research.
    • Identify new methodologies and innovative technologies of relevance for the expansion of flow cytometry services.
    • Provide scientific training to internal staff and provide scientific materials to other divisions as needed.
    • Maintain personal knowledge on therapeutic areas for which the technology platform is key.
  • Driver for Growth
    • Identify possible areas of improvement in how we work with partner laboratories, according to partners' needs and ensuring best alignment.
    • Identify and produce scientific and technical material to build capabilities awareness.
    • Identify new methodologies and innovative technologies of relevance.
    Requirements
    • PhD degree in Immunology or Oncology or related field of study.
    • More than 5 years of Flow Cytometry experience, including minimum of 2 years of Spectral Flow cytometry experience.
    • Work experience in pharma/biotech and/or CRO.
    • Understanding of CAP/CLIA, GCLP, and quality assurance for clinical laboratory and clinical testing.
    • Good communication and stakeholder management skills.
    • Good organizational skills.
    • Expertise in MS Office applications.
    • Project management experience.
    • Scientific writing skills.