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Director of R&D

United Kingdom, Liverpool · Job Posted June 14, 2026
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Job Description

Drive the future of clinical diagnostics through innovative assay development and scientific leadership. Proclinical is seeking a Director of R&D to lead the development of clinical assays and companion diagnostics (CDx) within the immuno-oncology and pharmaceutical space. This role focuses on advancing flow cytometry-based diagnostic tools from concept through validation and commercialization. The position requires a strong background in clinical assay development within a regulated IVD environment and offers the opportunity to shape long-term diagnostic innovation strategies. Travel across the UK, Spain, and wider Europe may be required.

Job Responsibility

  • Act as the technical and scientific authority for clinical flow cytometry assay and CDx development, guiding projects from feasibility to commercialization
  • Lead assay design, optimization, analytical performance characterization, verification, and validation to ensure clinical relevance and compliance
  • Assess project feasibility, identify risks, and propose solutions
  • Ensure scientific rigor during technical and design reviews
  • Oversee compliance with regulatory standards and documentation requirements
  • Collaborate across functions to align on execution strategies and plans
  • Mentor junior team members and facilitate training sessions to grow technical capabilities
  • Represent the organization at conferences, scientific meetings, and with regulatory agencies
  • Incorporate customer perspectives into product development processes
  • Stay updated on emerging trends and identify promising new technologies or assays
  • Contribute to business and portfolio strategy, supporting investment decisions and external engagements

Requirements

  • Advanced degree (Master's, MD, or PhD) in a relevant scientific field
  • Extensive experience in developing and commercializing clinical assays, ideally within an IVD or CDx environment
  • Strong expertise in flow cytometry applications and data analysis
  • Proven track record in clinical diagnostic R&D within an industry setting
  • Analytical and technical problem-solving skills
  • Ability to work effectively in cross-functional and geographically diverse teams
  • Excellent verbal, written, and presentation skills
  • Experience engaging with regulatory bodies and understanding regulations related to IVD and medical devices (e.g., 21 CFR, CE-IVD, ISO 13485)

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