Senior Scientist In Vivo Discovery

4 weeks ago


Cambridge, Massachusetts, United States Editas Medicine Full time
About the Role

We are seeking a highly motivated and skilled Associate Scientist II to join our In Vivo Discovery team at Editas Medicine. As a key member of our team, you will be responsible for developing and optimizing molecular assays for evaluating editing outcomes of CRISPR-based therapeutics in an in vivo context.

Key Responsibilities:

  • Development and optimization of molecular assays for evaluating editing outcomes of CRISPR-based therapeutics in an in vivo context.
  • Work with primary cells and cell lines.
  • Develop and perform in vitro cell-based assays supporting the pharmacology of CRISPR-based therapeutics.
  • Support in vivo studies for evaluation of LNP targeting and biodistribution.
  • Maintain an electronic lab notebook in a timely fashion.
  • Analyze and present data within the organization.
  • Collaborate with internal teams to develop assays for robust detection of LNP cargo, LNP dynamics, and LNP targeting.

Requirements:

  • BS/MS in Biology or related discipline and 6+/4+ years of hands-on research experience in academic and/or pharmaceutical/biotech environment.
  • Skilled in molecular assays including PCR and flow cytometry. Demonstrated knowledge in assay development and optimization.
  • Cell culture experience and experience with cell-based assays.
  • Animal handling experience is a must.

What We Offer:

  • A comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.

About Editas Medicine:

Editas Medicine is a pioneering company in the field of gene editing, committed to translating the power and potential of CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.


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