Abstract

Principal/Senior Scientist, PK/PD Assays

$155K–$200KFull-time · South San Francisco
✓ Verified live on the employer's own system · added 113 days ago
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Mid-level · 5+ yrs exp

Requirements

Education: Doctorate or related field

Experience: 5+ years

Skills & tools

Assay DevelopmentData AnalysisCell CultureTeam LeadershipResearchMolecular BiologyBiochemistryIch Guidelines

Benefits — mentioned in this posting

Equity / stockHealth, dental & vision401(k) / retirementFamily / parental leavePaid time off
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Full job description

What you'll do - Own the end-to-end design, development, and qualification of PK and PD biomarker assays across various platforms to support preclinical and IND-enabling studies - Discover and validate pharmacodynamic biomarkers to support the clinical development of drugs across multiple programs - Drive data analysis, interpretation, and reporting for bioanalytical studies to support program decision-making with audit-ready data packages - Contribute to sample processing workflows including tissue harvesting, primary cell culture, and complex matrix handling - Mentor research associates, establish SOPs, and build institutional knowledge within the bioanalytical function

Requirements - PhD in molecular biology, biochemistry, cell biology, or a related field or equivalent industry experience (5+ years) - 3+ years of hands-on experience in various quantitative bioanalytical assay platforms (e.g., RT-qPCR, ddPCR, ELISA, MSD, Olink, SOMAscan, NGS-based methods) in complex biological matrices (serum, plasma, tissue homogenates) - Strong working knowledge of bioanalytical method qualification/validation principles for PK/PD biomarker measurements, including familiarity with ICH M10 guidelines and fit-for-purpose frameworks - History of delivering results for bioanalytical projects -- you've discovered a PD biomarker or built an assay and solved all the problems along the way - Experience with primary cell culture and tissue-derived sample workflows Nice to have - Track record of bioanalytical method transfer and CRO management for outsourced projects - Familiarity with preclinical drug development timelines and regulatory submissions (IND, TGA, CTD format) - Experience with mRNA-LNP biodistribution or nucleic acid-based PK assays - Experience developing products in emerging therapeutic modalities (gene therapy, nucleic acid therapies, cell therapy)

Benefits NewLimit provides generous benefits so our team can remain focused on our mission: - Comprehensive Health, Dental, and Vision insurance - 401(k) plan with company match - Paid parental leave - Industry-leading PTO: 20 days per year plus holidays - On-site meals and snacks Salary Range: $155,000 to $200,000.

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. NewLimit offers a competitive benefits package, which includes a 401k, healthcare coverage, and 20 days of PTO. Learn more at: https://www.newlimit.com/careers *This compensation and benefits information is based on Company's good faith estimate as of the date of publication and may be modified in the future.

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This posting was published by Abstract on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.