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Precision for Medicine

Global CRO for precision medicine trials

Flow Cytometry Scientist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeFrederick, MD, USANo salary listedIn-person

About the Job

Requirements

  • A Master's degree in life sciences or another relevant field is required.
  • Five years of relevant laboratory experience is required.
  • Expert-level flow cytometry skills using both whole blood and isolated cells are required.
  • Demonstrated skills monitoring cell-mediated immunity through flow cytometry, ELISpot, ELISA, and MSD are required.
  • The ability to organize and analyze data and prepare reports is required.
  • Strong computational skills are required, preferably with experience using Word, Excel, PowerPoint, GraphPad Prism, Diva, and FlowJo.
  • The ability to read, write, speak fluently, and comprehend English is required.
  • The ability to see and differentiate colors across the full color spectrum is required.
  • The role may occasionally require extended work hours to meet business demands.
  • The role requires lifting and carrying 1–15 pounds and lifting up to 50 pounds overhead with assistance; frequent sitting, grasping, and right- or left-finger dexterity; and possible exposure to freezer temperatures from -20°C to -196°C.

Responsibilities

  • Perform flow cytometry and other immune assays.
  • Design and perform experiments, independently analyze data accurately, and present findings.
  • Maintain high-quality output and build efficiency to improve productivity metrics.
  • Assist in establishing and improving procedures and required standard operating procedure documentation.
  • Troubleshoot and correct routine scientific issues and problems.
  • Identify, update, and implement emerging laboratory techniques.
  • Maintain and support safe laboratory practices and the laboratory environment.
  • Collaborate with other technical teams to share resources and provide technical expertise.
  • Support operational qualification and performance checks for new equipment.
  • Monitor expenses related to Product and Service/R&D projects.
  • Serve as a scientific resource for clients and internal teams.
  • Assist with writing, reviewing, and editing contract and grant applications or proposals as appropriate.
  • Assist with writing and publishing papers, abstracts, techniques, or chapters to maintain scientific standards.
  • Present completed work at appropriate scientific meetings and in publications as appropriate.
  • Perform other duties as assigned.

Desired Qualifications

  • A solid understanding of current GLP or CAP/CLIA/ISO standards is preferred.
  • Demonstrated skills with immunophenotyping assays, such as primary cell-based assays, ELISpot, ELISA, and Mesoscale, are preferred.
  • Experience with cell-sorting techniques is preferred.

About the Company

Precision for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$225M
Headquarters
Bethesda, MD
Founded
2012

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