P

Precision for Medicine

Global CRO for precision medicine trials

Scientist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • A Master’s degree in life sciences or another relevant field.
  • Five years of relevant laboratory experience.
  • Expert-level flow cytometry skills using both whole blood and isolated cells.
  • Demonstrated skills monitoring cell-mediated immunity through flow cytometry, ELISpot, ELISA, and MSD.
  • Ability to organize and analyze data and prepare reports.
  • Computational skills; preferred tools include Word, Excel, PowerPoint, GraphPad Prism, Diva, and FlowJo.
  • Ability to read, write, speak fluently, and comprehend English.
  • Ability to differentiate colors across the full color spectrum.
  • Ability to lift and carry 1–15 pounds and, with assistance, lift up to 50 pounds overhead; frequent sitting, grasping, and finger dexterity are required.
  • May be exposed to freezer temperatures ranging from -20°C to -196°C.
  • Occasional extended work hours may be necessary to meet business demands.

Responsibilities

  • Perform flow cytometry and other immune assays.
  • Design and perform experiments, then accurately analyze and present data independently.
  • Produce high-quality work and build efficiency to improve productivity metrics.
  • Assist in establishing and improving procedures and required standard operating procedure documentation.
  • Troubleshoot and correct routine scientific issues and problems.
  • Identify, update, and implement emerging laboratory techniques.
  • Maintain and support safe laboratory practices and the laboratory environment.
  • Collaborate with other technical teams to share resources and provide technical expertise.
  • Support new equipment operational qualifications and performance checks.
  • Monitor product and service/research and development project expenses.
  • Serve as a scientific resource for external clients and internally.
  • Assist with writing, reviewing, and editing contract and grant applications or proposals as appropriate.
  • Assist with writing and publishing papers, abstracts, techniques, or chapters to maintain the company’s scientific standard and image.
  • Present completed work at appropriate scientific meetings and in publications as applicable.
  • Perform other duties as assigned.

Desired Qualifications

  • A solid understanding of current Good Laboratory Practice or CAP/CLIA/ISO standards.
  • Demonstrated skills with assays used for immunophenotyping, such as primary cell-based assays, ELISpot, ELISA, and Mesoscale.
  • Experience with cell sorting techniques.

About the Company

Precision for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$225M
Headquarters
Bethesda, MD
Founded
2012

Recently Posted Jobs

Explore more opportunities at Precision for Medicine

See more jobs