Nonclinical Bioanalysis Research Associate II

Planet Pharma

South San Francisco (CA)

On-site

USD 75,000 - 110,000

Full time

8 hours ago
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Job summary

Planet Pharma seeks a Research Associate II to support and execute nonclinical bioanalytical activities in GLP and non-GLP environments. You will process samples, run assays, analyze data, document results, and train other analysts in support of preclinical programs.

Based in South San Francisco, CA, this on-site role requires hands-on experience with qPCR/ddPCR, ELISA or MSD, and strong documentation practices. MS preferred and a proactive communicator will excel.

Qualifications

  • BS in Biology or related field (MS preferred).
  • Hands-on experience with qPCR/ddPCR, ELISA or MSD.
  • 5+ years in bioanalytical, molecular biology or related laboratory setting.
  • Experience following SOPs and study documentation.
  • GDP-compliant documentation practices.
  • Strong communication and organizational skills.

Responsibilities

  • Nonclinical bioanalytical activities in GLP and non-GLP environment.
  • Extract protein, DNA, and/or RNA from necropsied animal tissue.
  • Run ddPCR, qPCR, ELISA, MSD, Western blot, and related analyses on tissue extracts.
  • Perform nonclinical sample analysis.
  • Support drafting and maintenance of analysis plans and SOPs.
  • Data analysis, compilation, and QC.
  • Train and support other analysts on bioanalytical methods, workflows, and best laboratory practices.

Skills

qPCR/ddPCR, ELISA or MSD
GDP documentation
Communication skills
Organizational skills

Education

BS in Biology or related field
MS preferred

Tools

LIMS/ELN systems
Excel
SoftMax Pro
GraphPad Prism
JMP
SnapGene

Job description

Planet Pharma seeks a Research Associate II to support and execute nonclinical bioanalytical activities in GLP and non-GLP environments. You will process samples, run assays, analyze data, document results, and train other analysts in support of preclinical programs.

Based in South San Francisco, CA, this on-site role requires hands-on experience with qPCR/ddPCR, ELISA or MSD, and strong documentation practices. MS preferred and a proactive communicator will excel.

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