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Principal Scientist/Associate Director, Clinical Biomarkers

Principal Scientist/Associate Director, Clinical Biomarkers

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PRINCIPAL SCIENTIST / ASSOCIATE DIRECTOR, CLINICAL BIOMARKERS

Working closely with LTZ’s scientific and clinical teams, the Principal Scientist/Associate Director of Clinical Biomarkers will be the lead in the execution of scientific and strategic plans for translational studies of early-stage clinical trials. They will be responsible for the development and execution of clinical biomarker strategies, including the oversight of all cross-functional operational and scientific aspects of integrating biomarker assays into clinical trials.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:

Biomarker lead will be asked to:

• Develop, articulate, and lead the execution of actionable biomarker strategies across drug development stages, consistent with program development plans and regulatory strategies.
• Generate appropriate sections of project planning documents to outline, provide justification, and enable execution of the clinical biomarker strategy.
• Characterize tumor and immune profiling, pre- and post-treatment with myeloid cell activating bispecific antibodies.
• Oversee the development, validation, and execution of clinical biomarker assays, balancing the utilization of CRO’s and a strategic build-up and use of internal resources.
• Assess emerging technologies and establish technical platforms and assays to support biomarker research.
• Develop and direct scientifically accurate assays to translate preclinical data into clinical biomarkers for advancing LTZ’s clinical development program objectives.
• Contribute SME level knowledge of data, interpretation, and science to regulatory documents, investor communications, publications, etc.
• Communicate data and strategies to key internal and external stakeholders across LTZ.
• Other duties as required

EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS, AND ABILITIES

• PhD in immunology, cancer biology, or molecular and cellular biology with 5+ years of relevant experience in the biotechnology or pharmaceutical industry setting
• In-depth expertise in the development, execution, and oversight of biomarker plans for immuno-oncology clinical development
• Expertise in the development of biomarker assays and their implementation in clinical trials, and corresponding data analysis and interpretation
• Demonstrated scientific acumen and mechanistic understanding of cancer biology
• Ability to support and prioritize multiple projects as LTZ’s pipeline continues to evolve
• Ability to work in a fast-paced environment, driving strong science and results
• Demonstrated leadership, influencing, communication, and project management skills, with the ability to anticipate and solve problems.
• Experience and desire to motivate and develop others.

COMPENSATION

In addition to a competitive compensation package with stock options and a stock purchase plan, LTZ also offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance is also available.

JOB TYPE

• Full-time

BENEFITS

·Medical insurance

·Supplemental disability insurance plans

·Relocation assistance

WORK AUTHORIZATION

WORK LOCATION

EQUAL OPPORTUNITY EMPLOYER:

LTZ Therapeutics, Inc.is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity

CONTACTS

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

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