About The Position

The Research Scientist will support biomarker and translational strategy for the clinical development of Clien’s chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required.

Requirements

  • Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry or Master's Degree and 5+ years of scientific experience or Bachelor's Degree and 7+ years of scientific experience
  • Regulatory filing experience
  • Demonstrated ability to facilitate clinical trial execution
  • Demonstrated ability to synthesize scientific data
  • Demonstrated ability to communicate key findings cross-functionally

Nice To Haves

  • Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma
  • Prior experience in Regulatory filings
  • In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios
  • Strong understanding of clinical, translational, and mechanistic data
  • Familiarity and experience with clinical and biomarker operations
  • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia
  • Familiarity with bioanalytical assay development and validation in a GxP environment
  • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells
  • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities
  • Strong collaboration, excellent interpersonal and communication skills
  • Proficient with data presentations to communicate to a diverse cross-functional audience
  • Maintain a high degree of accuracy and attention to detail
  • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field)

Responsibilities

  • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma
  • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings
  • Reviews and contributes to clinical protocol design and study activities
  • Identify and establish agreements with contract research organizations (CRO) and support the transfer of novel methods
  • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data
  • Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries.
  • Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies
  • Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality
  • Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field
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