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Principal Scientist Assay Development Jobs (NOW HIRING)

WI · Hybrid

... including assay development, validation, CRO oversight, and deep data interpretation to support ... Conduct deep scientific review and interpretation of flow cytometry datasets to support PK/PD ...

The Research Scientist in Assay Development will design and execute experiments to functionalize sensors with nucleic acid or antibody probes for biomarker detection, contributing to the development ...

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Principal Scientist Assay Development information

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$68.5K

$144K

$190.5K

How much do principal scientist assay development jobs pay per year?

As of Jul 13, 2026, the average yearly pay for principal scientist assay development in the United States is $144,009.00, according to ZipRecruiter salary data. Most workers in this role earn between $117,500.00 and $169,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Principal Scientist Assay Development, and why are they important?

To thrive as a Principal Scientist Assay Development, you need advanced expertise in biochemistry or molecular biology, a PhD or equivalent experience, and a strong background in assay design and validation. Familiarity with laboratory automation, data analysis software, and regulatory compliance systems such as GLP/GMP is typically required. Leadership, project management, and effective communication are crucial soft skills for guiding teams and collaborating across departments. These skills ensure robust assay performance, regulatory adherence, and efficient innovation in complex scientific environments.

What is the difference between Principal Scientist Assay Development vs Senior Scientist Assay Development?

AspectPrincipal Scientist Assay DevelopmentSenior Scientist Assay Development
CredentialsAdvanced degree (PhD or equivalent), extensive experienceMaster's or PhD, significant industry experience
Work EnvironmentLeads assay development projects, strategic planningExecutes assay development tasks, supports project teams
Employer & Industry UsagePharmaceutical, biotech, CROs, biotech companiesPharmaceutical, biotech, research labs

The main difference between Principal Scientist Assay Development and Senior Scientist Assay Development lies in their level of responsibility and leadership. Principal Scientists typically lead projects, set strategies, and have more extensive experience, while Senior Scientists focus on executing assays and supporting project goals. Both roles require strong technical expertise, but the Principal Scientist position involves higher-level decision-making and oversight.

What are some common challenges faced by Principal Scientists in Assay Development, and how can they be addressed?

Principal Scientists in Assay Development often encounter challenges such as optimizing assay sensitivity and specificity, troubleshooting inconsistent results, and scaling up assays for high-throughput screening. Addressing these issues requires strong analytical thinking, effective cross-functional collaboration with research, engineering, and quality assurance teams, and staying updated with the latest technological advances. Regularly reviewing validation protocols and actively participating in peer discussions can also help in overcoming technical hurdles and ensuring robust assay performance.

What does a Principal Scientist in Assay Development do?

A Principal Scientist in Assay Development leads the design, optimization, and validation of assays used for research, diagnostics, or drug development. They oversee laboratory teams, develop protocols, and ensure that assays meet regulatory and quality standards. Their role also involves troubleshooting complex scientific problems, collaborating with cross-functional teams, and staying current with technological advances in assay technologies. Principal Scientists play a key role in translating scientific concepts into reliable, reproducible assays that support broader organizational goals.
More about Principal Scientist Assay Development jobs
What cities are hiring for Principal Scientist Assay Development jobs? Cities with the most Principal Scientist Assay Development job openings:
What states have the most Principal Scientist Assay Development jobs? States with the most job openings for Principal Scientist Assay Development jobs include:
Infographic showing various Principal Scientist Assay Development job openings in the United States as of July 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $144,009 per year, or $69.2 per hour.

Principal Scientist, Biomarker Assay Development Bench Scientist

Novartis Pharma Schweiz

Cambridge, MA

$126K - $234K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 19 hours ago

Posted today


Job description

Internal Position Title: Principal Scientist I/I

Location: Cambridge, MA. This role is based in Cambridge, MA. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Novartis Biomedical Research is seeking a highly skilled and motivated Principal Scientist (Level 4) to conduct bench research in a laboratory focused on preclinical and clinical biomarker assay development within Disease Area X (DAx). This position is integral to designing, developing, and qualifying biomarker assays that support drug discovery and development programs across DAx's diverse portfolio, including renal, liver, fibrosis, and exploratory indications. The successful candidate will work collaboratively within a matrixed team and contribute technical expertise to translational strategies that enable patient stratification and clinical impact.

Key responsibilities:
  • Design, develop, and qualify preclinical and clinical biomarker assays (cellular, soluble, proteomic, genetic, and genomic) to support target engagement, pharmacodynamics, and patient stratification for DAx programs.
  • The ideal candidate will bring deep technical and strategic expertise in designing, developing, optimizing, and clinically implementing ligand binding assays (e.g. ELISA, MSD, immunoassays).
  • Ensuring analytical rigor, robustness, and “fit-for purpose” performance expectations and technical assessment standards.
  • Execute laboratory‑based research, including hands‑on assay development, optimization, and troubleshooting.
  • Analyze and interpret experimental data, ensuring scientific rigor and reproducibility.
  • Collaborate with Translational Medicine, Biomarker Development, and DAx project teams to align assay strategies with DAx therapeutic area priorities.
  • Support the implementation of biomarker assays in preclinical and clinical studies, including documentation and reporting of results.
  • Maintain exemplary laboratory practices, including accurate record keeping and adherence to safety and regulatory guidelines.
  • Present research findings in lab meetings and contribute to scientific publications and internal reports.
Essential Requirements:
  • PhD or MD, Postdoctoral Fellowship preferred, with 4+ years’ experience in scientific and technical discipline of relevant field, or BS/MS with 8+ years’ experience in scientific and technical discipline of relevant field.
  • Hands‑on experience with designing and executing LBA assays.
  • Demonstrated experience in biomarker assay development, proteomics, genetics, genomics, or related fields within pharma or biotech.
  • Demonstrated expertise in assay development, qualification, and implementation for preclinical and/or clinical studies across various animal and human matrices.
  • Proven skill in independently developing and executing biochemical and cellular assays for drug discovery.
  • Innovative and critical thinking, with a track record of scientific impact and continuous improvement.
  • Excellent oral and written communication skills.
  • Commitment to scientific rigor, curiosity, and accountability in laboratory research.
Desirable Requirements:
  • Experience with multiomics profiling and patient stratification approaches, especially as applied to renal, liver, fibrosis, or exploratory disease areas.
  • Familiarity with animal models and ex vivo assays is a plus.
  • Hands‑on experience with RNA assays and/or LC‑MS based biomarker or assay quantification an added plus.
  • Knowledge of statistics and computational data analysis is desirable.
  • Experience working with CROs or external vendors to support assay development, biomarker studies or analytical deliverables.

The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and $126,000 and $234,000 per year for Principal Scientist II. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance‑based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US‑based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here.

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