Senior Scientist, Translational Immunology

Parvus Therapeutics Inc

$150K — $170K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree plus 10 years or Master's degree plus 6 years in Immunology or relevant life sciences.
  • At least 2 years of experience in a biotech or industry setting.
  • Expertise in high-dimensional flow cytometry assays like spectral flow cytometry and CyTOF.
  • Experience with clinical bioanalytical assay development and lab management.
  • Ability to create clinical biomarker budgets for early phase studies.
  • Strong communication and presentation skills.
  • Proven track record of collaborating in cross-functional teams.

Responsibilities

  • Identify and validate pharmacological biomarkers for clinical candidates.
  • Lead validation of clinical biomarker assays for phase 2 dosing and regulatory submissions.
  • Write and revise internal standard operating procedures and reports for compliance.
  • Collaborate with immunology and pharmacology teams on biomarker strategies for studies.
  • Participate in lab operations including training and compliance for audits.
  • Handle additional assigned duties as necessary.

Benefits

  • Opportunity to work in a dynamic and innovative biotech environment.
  • Exposure to cutting-edge research and development in immunology.
  • Collaboration with cross-functional teams to enhance professional growth.
  • On-site position facilitating teamwork and direct engagement with projects.
Full Job Description
Senior Scientist, Translational Immunology
Location: South San Francisco, CA (On-site)

The Position

We are seeking a Senior Scientist to join our team and drive projects enabling the translation, validation, and execution of preclinical biomarkers to the clinic.

Primary Responsibilities:
  • Identify and validate biomarkers relevant to the pharmacology of target clinical candidates.
  • Lead context-of-use validation (in-house or through CLIA-certified laboratories or clinical CROs) of clinical biomarker assays suitable for use in recommended phase 2 dosing selection and/or regulatory submission.
  • Write and amend internal SOPs and reports as necessary for GSP or GCLP purposes.
  • Liaise with nonclinical pharmacology and discovery immunology teams to establish proof-of-concept/proof-of-mechanism biomarker strategies suitable for use in NHPs and FIH studies.
  • Participate in all aspects of lab operation, training, and compliance including external audits where applicable.
  • Other duties and responsibilities as assigned.
Requirements:
  • Bachelors degree with a minimum 10 years of experience or a Masters degree with a minimum of 6 years of experience (at least 2 years must be in biotech or industry setting) in Immunology or other relevant life sciences. Experience with regulatory T cells or Tr1 cells will be prioritized.
  • Expertise in high-dimensional flow cytometry assays including but not limited to spectral flow cytometry and CyTOF.
  • Experience leading phase appropriate clinical bioanalytical assay development and analyses including full validation and management of clinical bioanalytical labs/CROs.
  • Experience developing lean and agile clinical biomarker budgets suitable for early phase POC and POM studies.
  • Nice to have:
    • Experience with nanomedicine
    • Experience with IQOQ
    • Familiarity with biomarker-centric platforms such as spatial profiling, multi-omics integration
  • Excellent oral, written communication, and presentation skills.
  • Demonstrated ability to effectively work in cross-functional teams, meet deadlines, and prioritize multiple projects is required.
  • Comfortable working collaboratively in a small, fast-paced environment.
  • Ability to quickly adjust to shifting project demands and priorities.
The expected annual salary range for this role is $150,000 - $170,000. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.

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