Senior Research Scientist, CRISPR screening operations

Broad Institute

$110K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. or equivalent in Cancer Biology, Molecular Biology, Biochemistry, Genetics, or related field.
  • 3+ years of experience with large-scale CRISPR or high-throughput screening.
  • Experience in a production-oriented lab environment, like a core facility.
  • Proven experience managing laboratory personnel.
  • Proficient in LIMS, electronic lab notebooks (ELNs), and project management tools.
  • Strong organizational and time management skills for concurrent projects.
  • Effective communicator across scientific and operational teams.

Responsibilities

  • Lead daily operations of CRISPR and high-throughput screening workflows as a production pipeline.
  • Develop and maintain standard operating procedures (SOPs) for experimental execution and data quality.
  • Manage project timelines, budgets, and resource allocation across multiple screens.
  • Supervise and mentor a team of research associates and coordinate with project teams.
  • Maintain comprehensive records in the Laboratory Information Management System (LIMS).
  • Ensure high-quality data delivery for analysis and downstream applications.
  • Continuously improve pipeline efficiency and scalability as screening volume increases.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan and flexible spending accounts.
  • At least 13 paid holidays and winter closure.
  • Generous paid time off and parental leave.
  • Employee assistance program and family care leave.
Full Job Description
The Broad Institute's Cancer Dependency Map ( DepMap), part of the Cancer Program, aims to comprehensively map cancer vulnerabilities using CRISPR-based functional genomics and other high-throughput screening methods to identify optimal therapeutic targets. DepMap leads the DepMap Consortium, a collaboration with leading pharmaceutical and biotech companies to build this pre-clinical resource, and is a key partner in PedDep, an initiative accelerating target discovery for childhood cancers.

We are seeking an experienced scientist to lead the day-to-day operation of our internal CRISPR screening and profiling platform. This is a production-focused role: you will run and manage large-scale screens as a reliable, high-throughput pipeline - similar to leading a core facility - rather than designing novel experiments.

You'll work closely with experimental scientists, project managers, and data analysts to keep screening data flowing on schedule and at a consistently high standard of quality.

The ideal candidate has hands-on experience running CRISPR screens at scale in a production or core-facility setting, and knows how to keep a pipeline running smoothly: staffing, SOPs, timelines, and quality control.

This role offers the chance to build deep expertise in functional genomics infrastructure within a leading cancer research program, with regular exposure to both academic and industry collaborators.

Key Responsibilities
  • Lead daily operations of large-scale CRISPR screens and other high-throughput screening workflows, treating screening as a production pipeline with defined throughput, quality, and turnaround targets.
  • Develop and maintain SOPs covering experimental execution, data acquisition, and quality control.
  • Manage project timelines, budgets, and resource allocation across concurrent screens.
  • Supervise and mentor a team of 2+ research associates; coordinate with scientists, project managers, and analysts to keep projects on track.
  • Maintain accurate records in the Laboratory Information Management System (LIMS) and ensure data is delivered in a form ready for downstream analysis.
  • Continuously improve pipeline efficiency, reproducibility, and scalability as screening volume grows.


Qualifications
  • Ph.D. or equivalent experience in Cancer Biology, Molecular Biology, Biochemistry, Genetics, or a related field.
  • 3+ years running large-scale CRISPR screens or other high-throughput screening methods.
  • Experience operating in a production-oriented lab environment (e.g., a core facility, screening center, or similar high-throughput operation).
  • Prior experience managing lab personnel.
  • Proficiency with LIMS, electronic lab notebooks (ELNs), and project management software.
  • Strong organizational skills and comfort managing multiple concurrent projects against fixed timelines.
  • Clear communicator, comfortable working across scientific, operational, and data teams.


The expected base pay range for this position as listed above is based on a 40 hour per week schedule. Broad provides pay ranges representing its reasonable and good faith estimate of what the organization reasonably expects to pay for a position at the time of posting. Actual compensation will vary based on factors including but not limited to, relevant skills, experience, education, qualifications, and other factors permissible by law.

At Broad, your base pay is just one part of a comprehensive total rewards package. From day one, this role offers a competitive benefits package including medical, dental, vision, life, and disability insurance; a 401(k) retirement plan; flexible spending and health savings accounts; at least 13 paid holidays; winter closure; paid time off; parental and family care leave; and an employee assistance program, among other Broad benefits.

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