Clinical Flow Cytometry Scientist

2 weeks ago

Reston, Virginia, United States Net2Source Inc. Full time

Job Title: Clinical Flow Cytometry Scientist

Location: Groton, CT

Duration: 18+ Month Contract

Payrate: $42/hr on w2 without benefits

Job Summary:

We are seeking a highly skilled Clinical Flow Cytometry Scientist to join our team at Net2Source Inc. in Groton, CT. As a key member of our Regulated Clinical Biomarker/Flow Cytometry group, you will be responsible for developing and implementing complex flow cytometry-based biomarker assays and supportive translational/mechanistic studies for early phase clinical projects in a GCLP environment.

Key Responsibilities:

  • Develop and validate clinical flow cytometry biomarker assays and data generation and analysis
  • Participate in ECD teams and research units in a matrix environment, demonstrating experience in delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in clinical studies
  • Develop partnerships in a matrix environment, influencing project strategies, and providing expertise in technology development and implementation
  • Participate in all phases of FACs laboratory operations, including technology evaluations, sample preparation, separation and detection methods, data analysis, interpretation, reporting, and follow-up discussions with project teams
  • Maintain regulatory compliance, including training and understanding of GLP/GCP guidance for execution of preclinical and clinical studies
  • Participate in continuous improvement of scientific and regulatory processes via update/creation of SOPs, design and implementation of laboratory and study-based processes, and development of best practices for bioanalytical data generation

Requirements:

• Strong knowledge of biological systems, cellular functions, and concepts in immunology

• Experience in delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in clinical studies

• Ability to work in a matrix environment, influencing project strategies, and providing expertise in technology development and implementation

• Strong analytical and problem-solving skills, with ability to interpret data and communicate results to project teams

• Ability to maintain regulatory compliance, including training and understanding of GLP/GCP guidance for execution of preclinical and clinical studies

What We Offer:

• Competitive payrate of $42/hr on w2 without benefits

• Opportunity to work in a dynamic and matrixed environment

• Professional development and growth opportunities

• Collaborative and supportive team environment

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