Pattern Biosciences
Lead the planning and execution of biomarker strategy and drive biomarker assay development for preclinical and clinical oncology studies using gene therapy modality. Collaborate with cross-functional teams and external partners to drive clinical biomarker innovation for cancer gene therapy programs, utilizing strong wet-lab and data analysis skills in a collaborative environment.
Key Responsibilities
- • Establish translatable biomarkers for preclinical and clinical development, including biomarkers for patient selection, drug response monitoring, pharmacodynamics and mechanism of action.
- • Design and validate biomarker assays, developing SOPs for robust and reproducible biomarker quantification using patient-derived specimens.
- • Contribute to biomarker strategy in clinical trials.
- • Work closely with the biospecimen team to optimize, standardize and document pre-analytical biospecimen handling and processing conditions to support the transition of biomarker assays into clinical trials.
- • Oversee and manage relationships with CROs and vendors for outsourced clinical biomarker assay development, validation, and regulatory compliance.
- • Analyze biomarker data to derive insights into patient response, pharmacodynamics, and mechanisms of action.
- • Collaborate with regulatory teams to ensure biomarker strategies align with clinical trial and regulatory submission requirements.
Required
- • PhD and/or MD with 3+ years of industry experience in oncology disease or cell/gene therapy (CGT).
- • Excellent understanding of drug development and regulatory processes.
- • Extensive hands-on experience developing biomarker assay protocols and analyzing patient specimens using techniques such as IHC/IF, ISH, ELISA and ELISPOT.
- • Experience leading biomarker assay outsourcing with external vendors/CROs.
- • Excellent written and communication skills.
- • Thrives in a fast-paced, high-growth environment with a track record of delivering results on time and within budget.
- • Proven ability to work independently and collaboratively in a team environment.
Company Overview
Industry: Healthcare Technology
Company Size: 500-1,000 employees
Founded: 2015
Headquarters: San Francisco, CA
Company Links
Key Contacts
Contact information not available
About the Company
Leading healthcare technology company focused on improving patient outcomes through innovative digital solutions. We're transforming the way healthcare is delivered with cutting-edge technology and data-driven insights. Our platform serves over 10,000 healthcare professionals and has processed millions of patient interactions.
Recent News & Updates
You will lead the planning and execution of biomarker strategy and drive biomarker assay development for preclinical and clinical oncology studies using gene therapy modality. In this role, you will collaborate with cross-functional teams and external partners to drive clinical biomarker innovation for cancer gene therapy programs. This is an ideal position for a highly motivated individual who has strong wet-lab and data analysis skills, and thrives in a cross-disciplinary and collaborative environment.
\n- Establish translatable biomarkers for preclinical and clinical development, including biomarkers for patient selection, drug response monitoring, pharmacodynamics and mechanism of action.
- Design and validate biomarker assays, developing SOPs for robust and reproducible biomarker quantification using patient-derived specimens. Contribute to biomarker strategy in clinical trials.
- Work closely with the biospecimen team to optimize, standardize and document pre-analytical biospecimen handling and processing conditions to support the transition of biomarker assays into clinical trials.
- Oversee and manage relationships with CROs and vendors for outsourced clinical biomarker assay development, validation, and regulatory compliance.
- Analyze biomarker data to derive insights into patient response, pharmacodynamics, and mechanisms of action.
- Collaborate with regulatory teams to ensure biomarker strategies align with clinical trial and regulatory submission requirements.
- PhD and/or MD with 3+ years of industry experience in oncology disease or cell/gene therapy (CGT).
- Excellent understanding of drug development and regulatory processes.
- Extensive hands-on experience developing biomarker assay protocols and analyzing patient specimens using techniques such as IHC/IF, ISH, ELISA and ELISPOT.
- Experience leading biomarker assay outsourcing with external vendors/CROs.
- Excellent written and communication skills.
- Thrives in a fast-paced, high-growth environment with a track record of delivering results
- on time and within budget
- Proven ability to work independently and collaboratively in a team environment.
At Pattern Bio, we design biological circuits at the intersection of synthetic biology and AI for cell-specific targeting of cancer tissue. By integrating data-driven design into every step—from DNA constructs to AAV-based delivery systems—we are building precise, rationally engineered, curative therapies. Our cohesive and driven team in South San Francisco is dedicated to curing cancer and saving lives.
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