CAR-T Translational Scientist for Multiple Myeloma

Unicon Pharma Inc

San Mateo (CA)

Hybrid

USD 130,000 - 180,000

Full time

20 hours ago
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Job summary

Unicon Pharma Inc. seeks a Research Scientist to advance biomarker strategies and translational medicine for CAR-T programs in Multiple Myeloma.

The role bridges Research and Clinical Development, engaging with cross-functional teams to shape biomarker plans and regulatory interactions. You will lead PK/PD guidance, contribute to protocols, analyze data, and support regulatory submissions while collaborating with external partners and KOLs.

Qualifications

  • Advanced degree in life sciences required.
  • Experience with oncology/immunology/cancer immunotherapy.
  • Experience with regulatory filings and clinical/translational development.
  • Knowledge of GxP biomarker operations and bioanalytical assays.
  • Experience with engineered T cells, immunophenotyping, or NGS.
  • Strong cross-functional communication and data presentation skills.

Responsibilities

  • Lead PK/PD and biomarker strategy for CAR-T trials.
  • Serve as Biomarker Lead on study teams and support filings.
  • Contribute to protocols, trial execution, data analysis, and regulatory responses.
  • Manage CRO collaborations and bioanalytical transfers.
  • Partner with Clinical Operations, Regulatory, Biometrics, Bioinformatics, and Translational teams.
  • Support biomarker, tumor biology, and CAR-T function studies.

Skills

PK/PD biomarker strategy
Regulatory filings experience
Cross-functional collaboration
Data presentation
Immunology/cancer immunotherapy

Education

PhD/MD/PharmD
MS
BS with experience

Job description

Unicon Pharma Inc. seeks a Research Scientist to advance biomarker strategies and translational medicine for CAR-T programs in Multiple Myeloma.

The role bridges Research and Clinical Development, engaging with cross-functional teams to shape biomarker plans and regulatory interactions. You will lead PK/PD guidance, contribute to protocols, analyze data, and support regulatory submissions while collaborating with external partners and KOLs.

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