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Senior Molecular Biologist

2 months ago

Lake Forest, California, United States Lucid Diagnostics Full time
About the Role

We are seeking a highly skilled Senior Molecular Biologist to lead the development of molecular diagnostic biomarker tests for early cancer detection at Lucid Diagnostics.

Key Responsibilities
  • Design, develop, and optimize genetic molecular diagnostic assays for early cancer detection, including biomarker discovery, assay validation, and clinical performance evaluation.
  • Develop innovative approaches to enhance the sensitivity, specificity, and robustness of diagnostic tests, ensuring alignment with regulatory requirements.
  • Conduct and oversee experiments to evaluate the feasibility and effectiveness of new molecular diagnostic technologies.
  • Manage multiple R&D projects simultaneously, ensuring timely completion of milestones and objectives.
  • Collaborate with cross-functional teams to advance diagnostic test development from bench to bedside.
  • Mentor and provide scientific guidance to junior scientists and research associates, fostering a collaborative and innovative research environment.
  • Stay abreast of the latest scientific and technological advancements in cancer diagnostics and molecular biology and integrate new knowledge into ongoing projects.
  • Communicate complex scientific concepts clearly and effectively through oral presentations and written reports.
Requirements
  • Ph.D. in Molecular Biology, Genetics, Cancer Biology, or a related field.
  • A minimum of 7-10 years of postdoctoral experience in molecular diagnostics, oncology, or a closely related area.
  • Extensive experience in developing genetic assays, including qPCR, NGS, and other molecular techniques.
  • Strong understanding of cancer biology, tumor genomics, and biomarkers relevant to early cancer detection.
  • Proven experience in genetics, proteomics, epigenetics research related to cancer diagnostics.
  • Track record of leading successful R&D projects, with a portfolio of peer-reviewed publications and patents.
  • Experience with regulatory standards for diagnostic test development, including CLIA, CAP, and FDA regulations.
  • Excellent leadership, communication, and project management skills.
  • Ability to work effectively and collaboratively with multi-disciplinary teams.
Preferred Qualifications
  • Experience in liquid biopsy, miRNA analysis, ctDNA analysis, and other non-invasive diagnostic technologies.
  • Knowledge of bioinformatics tools and software for genetic data analysis.
  • Previous experience in a leadership role within the biotech or diagnostics industry.