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Research Scientist - MCED

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Exact Sciences

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Location:
United States , San Diego

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

100000.00 - 150000.00 USD / Year
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Job Description:

The Research Scientist, with limited guidance from more experienced scientists, works individually and in collaboration with others on multiple projects which are moderate to complex in scope. The Research Scientist plays an active role in planning of projects and experiments and is often the technical lead responsible for the successful execution of the project. This position involves independently making detailed observations, analyzing data and interpreting results. Working in a team setting, the Research Scientist, will primarily be involved in Research and Development projects serving as a technical lead in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products for cancer screening.

Job Responsibility:

  • Conduct bench level experiments within several product or technology areas and identify problems and discrepancies
  • Independently plan and analyze results of bench level experiments within several product or technology areas
  • effectively present at data meetings, group meetings, and project team meetings
  • Operate scientific instrumentation related to performance of duties and notify appropriate personnel of any problems
  • Effectively utilize and apply methods or technologies and provide ideas for new techniques, when appropriate
  • Maintain knowledge of technological industry developments that could assist in completion of an assignment or aid in the development of new processes or procedures
  • Provide technical input and participate in decisions affecting project planning and experimental design
  • Prepare and provide information and data for scientific abstracts/conferences/project meetings/publication
  • Generate, document, and communicate development plans for critical aspects of a project
  • Participate in the development of research plans and experimental outlines, write experimental protocols, and perform laboratory experiments
  • Prepare detailed technical procedures, protocols, and reports
  • Evaluate impact of nonconforming data to product or process
  • Identify and address trends in study data
  • Prepare and approve written reports
  • Lead identification of areas for process improvements
  • Maintain lab notebook in a complete and consistent manner, following all legal, ISO, and QSR requirements, as well as keeping clear and complete
  • Prepare reports and documentation providing the analysis or summarization of experimental results, outcomes, and next steps to supervisor, technical teams/groups, or project teams
  • Present experimental results and defend scientific ideas and findings at project or departmental meetings
  • provide technical input, as needed
  • Work on problems of diverse and complex in scope in which analysis of data requires evaluation of identifiable factors
  • Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions
  • Work on individual assignments and with project team members, as appropriate, to meet department and project objectives
  • Work within project timeframes that are established collaboratively by team members
  • Act as technical leader for one or more projects that are moderate to complex in scope
  • Exercise discretion and independent judgement within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining and interpreting results, analyzing data, and presenting findings in a professional and knowledgeable manner
  • Promote an open, collaborative environment built on trust to foster positive teamwork
  • Assist in planning and recommendation of activities that account for prioritization of organizational and department goals
  • Ability to train and mentor research associates
  • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork
  • Support and comply with the company’s Quality Management System policies and procedures
  • Regular and reliable attendance

Requirements:

  • PhD in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field
  • or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 4 years of related experience in lieu of a PhD
  • or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or related field and 6 years of related experience in lieu of PhD
  • 1+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
  • Demonstrated ability to apply molecular biology and/or biochemical techniques
  • Demonstrated understanding of GMP, ISO, and Quality Systems
  • Good knowledge of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics
  • Basic knowledge of statistical and mathematical methods in biology/genetics/genomics
  • including experience with statistical software, such as JMP
  • Proficient computer skills to include Internet navigation, Email usage, and word processing
  • Proficient in Microsoft Office to include Excel, Word, and PowerPoint
  • Demonstrated ability to perform the Essential Duties of the position with or without accommodation
  • Authorization to work in the United States without sponsorship

Nice to have:

  • Experience with genomic databases and related software
  • Previous experience working in a molecular diagnostics/clinical laboratory setting
  • Understanding of the practices and principles of NGS including molecular biology and data analysis based upon extensive hands-on experience with the development, optimization and troubleshooting of NGS-based workflows for DNA and RNA from clinical samples
  • Experience with interpretation and analysis of NGS data using external and in-house computational methods to support method development and characterization of genomic and epigenomic biomarkers associated with cancer
  • Experience with product development for use in an LDT/IVD- or FDA-regulated environment including designing analytical validation studies, ideally in medical device development
  • Diagnostic/Therapeutic product development experience
What we offer:
  • Paid time off (including days for vacation, holidays, volunteering, and personal time)
  • Paid leave for parents and caregivers
  • A retirement savings plan
  • Wellness support
  • Health benefits including medical, prescription drug, dental, and vision coverage
  • Bonus eligibility

Additional Information:

Job Posted:
January 24, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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