Research Associate/Senior Research Associate, Analytical Development

Posted 24 Days Ago
Be an Early Applicant
Boston, MA
1-3 Years Experience
Healthtech • Biotech • Pharmaceutical
The Role
Seeking a Senior Research Associate/Research Associate in Cell Biology and Potency Analytics to support analytical method development and testing of mRNA and gRNA oligonucleotide drug substances and drug products. Responsibilities include collaborating across teams, drafting analytical test methods, developing cell-based potency assays, authoring SOPs, and other duties as assigned.
Summary Generated by Built In
The Company

Verve is a clinical-stage genetic medicines company established with a mission to solve the global health epidemic of cardiovascular disease. Founded by world-leading experts in cardiovascular medicine, human genetics and gene-editing, Verve is pioneering a new approach to the care of cardiovascular disease, potentially transforming treatment from chronic management to single-course gene editing medicines. The company’s initial three programs – VERVE-101, VERVE-102, and VERVE-201 – target genes that have been extensively validated as targets for lowering low-density lipoprotein cholesterol (LDL-C), a root cause of cardiovascular disease. VERVE-101 and VERVE-102 are designed to permanently turn off the PCSK9 gene in the liver and are being developed initially for heterozygous familial hypercholesterolemia (HeFH) and ultimately to treat atherosclerotic cardiovascular disease (ASCVD) patients not at goal on oral therapy. VERVE-201 is designed to permanently turn off the ANGPTL3 gene in the liver and is initially being developed for homozygous familial hypercholesterolemia (HoFH) and ultimately to treat patients with refractory hypercholesterolemia. In 2023, Verve was named a Top Place to Work by The Boston Globe for the third consecutive year. Verve is headquartered in Boston, Massachusetts.

The Position

Verve is seeking a Senior Research Associate/Research Associate in Cell Biology and Potency Analytics to support analytical method development and testing of mRNA and gRNA oligonucleotide drug substances and drug products across all stages of development.  This individual will be working in a cross-functional team to design, develop and qualify phase appropriate bioassays to support Verve’s growing gene editing pipeline.  The position will be part of an integrated project team that aims to advance preclinical gene editing candidates into the clinic and work closely with discovery, process development and internal quality control groups.

Job Responsibilities

  • Collaborate across multiple cross- functional teams to perform experiments and summarize work in presentations and technical reports.
  • Draft analytical test methods, maintain equipment and order critical reagents.
  • Develop and apply cell-based potency assays, immunoassays, and other state of the art technologies to analyze and characterize cell and gene products.
  • Author Standard Operating Procedures (SOPS), test methods, and generate qualification protocols and reports.
  • Other duties as assigned.

Qualifications

  • B.S. degree in biological sciences / pharmaceutical sciences or related scientific concentration. (3+ years of related experience for Senior Research Associate level).
  • Previous experience in gene therapy method development and/or qualification is a plus.
  • Knowledge/hands-on experience in cell biology techniques and assays are a plus, but not required.
  • Ability to work effectively on cross-functional teams with a willingness to roll-up-sleeves to get things done.
  • Excellent interpersonal and collaborative skills, and the ability to work independently and effectively in a highly dynamic environment.
  • Comfortable communicating highly technical information.
  • Strong attention to detail, critical analysis of data/reports, and sound troubleshooting abilities.

Don’t check off every box in the requirements listed above?  Please consider applying anyway. We want the best candidates for the job, and those candidates don’t always meet 100% of the qualifications listed. At Verve, we are dedicated to building diverse and inclusive teams who embody the values we share: grit, spirit, drive, and passion. We look forward to learning more about your unique background.

EEO Statement

Verve Therapeutics is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability or special need that requires accommodation, please let us know.

Recruitment & Staffing Agencies

Verve Therapeutics does not accept agency resumes unless contacted directly by internal Verve Talent Acquisition. Please do not forward resumes to Verve employees or any other company location; Verve Therapeutics is not responsible for any fees related to unsolicited resumes.

The Company
Boston, Massachusetts
284 Employees
On-site Workplace
Year Founded: 2018

What We Do

Verve Therapeutics is a clinical-stage biotechnology company created with a singular focus: to protect the world from heart disease. Founded by world-leading experts in cardiovascular medicine, human genetics and gene editing, the company aims to develop transformative, once-and-done therapies for coronary heart disease. Verve’s gene editing medicines are designed to safely edit the genome of adults and mimic naturally occurring gene variants to permanently lower LDL cholesterol and triglyceride levels. The company is advancing a pipeline of precision genetic medicines, led by VERVE-101, which is being developed initially for heterozygous familial hypercholesterolemia, a potentially fatal genetic heart disease. In 2023, Verve was recognized as a "Best Places to Work" by the Boston Globe. Verve is headquartered in Boston, Massachusetts

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