Principal Scientist/Associate Director, Translational Sciences
- Design and execute translational biomarker strategies to support mechanism-of-action, PK/PD, dose predictions, and patient stratification in Phase I/II first-in-human oncology trials.
- Integrate preclinical and clinical data to generate hypotheses and guide data-driven decision-making in early development.
- Lead development and implementation of exploratory and translational biomarkers, including immune profiling, ctDNA, and genomic assays, with a strong understanding of solid tumor biology.
- Evaluate and oversee protein biomarker assays relevant to therapeutic response and resistance.
- Manage external vendors and CROs for biomarker assay development, sample testing, and data delivery; ensure high-quality execution and troubleshooting as needed.
- Oversee sample logistics (tumor tissue, liquid biopsies) to ensure integrity and timely analysis.
- Partner closely with Clinical Development and Discovery Research teams to ensure translational plans align with clinical objectives and regulatory strategies.
- Work closely with leadership to develop, manage, and deliver translational research timelines, budgets, metrics, and milestones.
- Demonstrate a strong work ethic and ability to work well in team environment.
- Communicate key findings and recommendations to senior leadership.
- PhD, MD, or equivalent in cancer biology, oncology, immunology, molecular biology, or related field.
- 8+ years of biotech/pharma experience in translational sciences or biomarker research, ideally in a biotech or pharmaceutical environment.
- Deep understanding of solid tumor biology, immune biomarkers, and ctDNA/genomic analysis, along with hands-on experience managing biomarker execution in early-phase clinical trials.
- Strong understanding of drug development for protein therapeutics and immune-oncology mechanisms.
- Demonstrated experience supporting Phase I/II first-in-patient clinical studies.
- Experience incorporating ctDNA endpoints into Phase I/II oncology clinical trials, including exploratory biomarker strategies and regulatory considerations.
- Experience transferring and overseeing assays at CROs or central labs.
- Working knowledge of pharmacokinetics (PK) and anti-drug antibody (ADA) assessments for protein therapeutics, and ability to integrate PK/ADA findings with biomarker and clinical data to guide early development decisions.
- Hands-on or oversight experience with circulating tumor DNA (ctDNA), including use in solid tumor clinical trials for patient stratification and treatment response monitoring.
- Entrepreneurial mindset, excellent communication skills, and passion for advancing new therapies for patients.
Repertoire is committed towards social responsibility and developing an inclusive culture. Much as the power of the immune system lies in the diversity of T and B cells, our work requires the creativity and ingenuity of a diverse workforce. We believe in actively pursuing equity in all facets of the work experience at Repertoire. We will continue to educate ourselves about the inequities and barriers present in our society and take action as a company where we can make a difference.
Repertoire is proud to be an Equal Opportunity Employer.
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