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Precision for Medicine

Global CRO for precision medicine trials

Associate Scientist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeFrederick, MD, USA

About the Job

Requirements

  • A Bachelor's degree with eight years of relevant laboratory experience in an acceptable laboratory, or a Master's degree with at least two years of relevant laboratory experience in an acceptable laboratory.
  • A Bachelor's or Master's degree from an accredited institution with a major in chemical, biological, clinical, or medical sciences, or medical technology.
  • Expert-level mammalian cell culture and plate-based cellular assay experience.
  • Ability to organize and analyze data and prepare reports.
  • Strong computational skills, preferably including experience with Word, Excel, PowerPoint, and GraphPad Prism.
  • Ability to read, write, speak fluently, and comprehend English.
  • Ability to work extended hours occasionally to meet business demands.
  • Ability to lift and carry 1–15 pounds and lift up to 50 pounds overhead with assistance; frequent sitting, grasping, and right/left finger dexterity are required; may be exposed to freezer temperatures from -20°C to -196°C.

Responsibilities

  • Perform Neutralizing Antibody Assays primarily, as well as other immunocellular assays.
  • Design and perform experiments and independently analyze and present data accurately.
  • Produce high-quality work and build efficiency into improving productivity metrics.
  • Assist in establishing and improving procedures and required SOP 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 in resource sharing and providing technical expertise.
  • Support new equipment operational qualifications and performance checks.
  • Monitor Product and Service/R&D-related project expenses.
  • Act as a scientific technology platform lead externally to clients and internally.
  • Assist with writing, reviewing, and editing contract and grant applications or proposals as appropriate.
  • Write and prepare abstracts, techniques, or draft scientific papers to maintain the scientific standard and image of the company.
  • May present completed work at appropriate scientific meetings and in publications.
  • Perform other duties as assigned.
  • Work a Tuesday-through-Saturday schedule to support cellular activities and maintain operational continuity.
  • When qualified and designated, serve as a Clinical Laboratory General Supervisor, providing day-to-day oversight of testing activities in accordance with CLIA/CAP, ISO, and New York laboratory policies.

Desired Qualifications

  • A solid understanding of current GxP and CAP/CLIA/ISO/New York clinical laboratory standards.
  • Demonstrated skills with assays used for immune monitoring, such as Total Antibody Detection, cell-based Neutralizing Antibody, and functional cytokine production assays.

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

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