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Clinical Research Associate

4 months ago


Norwood, United States Randstad USA Full time

Research Associate - Molecular Assays

Pay Rate 35-39 per hour

Onsite in Norwood, MA

Contract to start

  • 2 years of experience in Next Generation Sequencing & RNA sequencing. Experience with Clinical samples & GxP a plus


Moderna is seeking a highly motivated and detail-oriented Research Associate I, Molecular Assays (Contractor) to join the Clinical Bioanalytical and Molecular Assays team. A successful incumbent would help integrate basic science research, bioanalysis, genomics and informatics to move programs into the clinic as well as reverse-engineer clinical findings to novel opportunities for Moderna’s pipeline. This position offers an excellent opportunity to work in a dynamic and collaborative environment, contributing to cutting-edge scientific research.


Here's What You’ll Do:

  • Take part in the design and effective execution of phase-appropriate biochemical and molecular biology assays to enable pharmacokinetic/pharmacodynamic (PK/PD) analysis,
  • including genomic DNA and RNA isolation, qPCR, ddPCR, NGS sequencing, and other relevant technologies.
  • Work with manager to ensure assays are developed in a timely manner to meet program timelines, the qualification or validation of assays is fit for purpose within GcLP compliance for clinical use and troubleshoot any issues.
  • Analyze and interpret experimental data, ensuring accuracy and reproducibility of results.
  • Maintain detailed and accurate records of experimental procedures, results, and observations in electronic lab notebooks and Watson LIMS system.
  • Responsibilities also include analytical equipment procurement/qualifications, preparation and maintenance of SOP’s, determination, and control of critical reagents for example.
  • Must follow government guidelines, internal guidance on clinical trial conduct including Good Laboratory Practice (GLP), Good Clinical Practice (GCP), internal SOPs and regulations and White Papers, as appropriate, for clinical bioanalysis to ensure practices are consistent with regulatory expectations.
  • Work closely with cross-functional teams, including molecular biologists, bioinformaticians, and project managers, to achieve project goals.


Here’s What You’ll Bring to the Table:

  • Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Genetics, or a related field. 0-2 years of hands-on experience in molecular biology and other relevant
  • Experience with PCR, RT-qPCR, ddPCR nucleic acid extraction, and other molecular biology techniques.
  • Knowledge on Next Generation Sequencing would be helpful.
  • Excellent written and verbal communication skills.
  • Ability to work effectively both independently and as part of a team.
  • Flexibility to adapt to changing priorities and project timelines
  • Knowledge on working in a regulatory laboratory