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Katalyst Healthcare & Life Sciences

Clinical trial management software and consulting

Scientist 3 - Biotherapeutics and Genetic Medicine

Translational Research & Bench BiologyConfirmed live in the last 24 hours
Full-timeWorcester, MA, USANo salary listedIn-person

About the Job

Requirements

  • A Ph.D. in biology or a relevant field with at least 5 years of experience in lentiviral vector-based gene therapy in addition to post-doctoral experience, or an MS with at least 10 years of relevant experience.
  • Strong expertise and experience in lentiviral vector design, engineering, and production.
  • Experience managing contract research organizations for lentiviral production.
  • Experience with analytical and screening methods for characterization of lentiviral vector products, including experience in CAR-T cell therapy.
  • Ability to work effectively in a highly collaborative and dynamic environment.
  • Excellent verbal and written communication skills.
  • Excellent organization and collaborative skills.
  • Attention to detail and a commitment to delivering quality results.

Responsibilities

  • Collaborate with cross-functional and therapeutic area teams to advance the client's lentiviral vectors into the pipeline.
  • Design and engineer lentiviral vectors and manage lentiviral production using internal and contract research organization resources.
  • Help build and establish analytical and cell-based screening assays, including p24, vector copy number, SupT1 titration, enzyme-linked immunosorbent assay, quantitative polymerase chain reaction, droplet digital polymerase chain reaction, whole-exome sequencing, fluorescence-activated cell sorting, and endotoxin assays.
  • Maintain a comprehensive electronic laboratory notebook documenting experiments.
  • Maintain clear, daily, detailed, and accurate documentation of experiments.
  • Author technical reports and protocols.
  • Understand and enforce company culture, teamwork, safety, and appropriate handling of materials in a Biosafety Level 2 environment.
  • Perform all activities in compliance with applicable regulations and the client's policies and guidelines.
  • Perform other assigned responsibilities.

Desired Qualifications

  • Industrial experience is highly desired.
  • Experience in in vivo lentiviral targeted delivery is a plus.

About the Company

Katalyst Healthcare & Life Sciences

Clinical trial management software and consulting

Katalyst Healthcare & Life Sciences offers EasyCDM Suite, a Clinical Trial Management Solution paired with consulting services to manage the full trial lifecycle. The platform covers study design, electronic data capture, medical coding, and data management, with implementation and optimization support from a consulting team. It differentiates itself by providing an all-in-one, configurable suite combined with industry-specific consulting across pharma, biopharma, medical devices, cosmeceuticals, and food/bev sectors. Its goal is to simplify business challenges and accelerate safe, effective development to improve global health.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
South Plainfield, NJ
Founded
2016

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