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Bioanalytical Cro information

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$24K

$58.4K

$135K

How much do bioanalytical cro jobs pay per year?

As of Jun 6, 2026, the average yearly pay for bioanalytical cro in the United States is $58,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,500.00 and $69,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by bioanalytical CRO professionals, and how can they be addressed?

Professionals working in bioanalytical CROs often encounter challenges such as managing tight project timelines, ensuring regulatory compliance, and adapting to rapidly changing client requirements. Balancing multiple studies simultaneously requires strong organizational skills and effective communication with both internal teams and clients. To address these challenges, it is important to maintain clear documentation, stay updated on industry best practices, and foster a collaborative team environment to ensure high-quality, reproducible results.

What is the difference between Bioanalytical Cro vs Bioanalytical Scientist?

AspectBioanalytical CroBioanalytical Scientist
CredentialsTypically requires a degree in life sciences, pharmacology, or related fields; certifications vary by companyRequires a degree in biology, chemistry, or related fields; advanced degrees preferred
Work EnvironmentContract research organizations, pharmaceutical companies, or biotech firms; project-based workResearch labs, pharmaceutical companies, or academic settings; more independent research
Employer & Industry UsageCommonly hired for clinical trial support and regulatory studiesEngaged in experimental design, data analysis, and method development

While both roles require a background in life sciences, a Bioanalytical Cro primarily manages outsourced projects and client communication, whereas a Bioanalytical Scientist focuses on experimental work and data analysis within a lab setting.

What are bioanalytical CROs?

Bioanalytical CROs, or Contract Research Organizations, are specialized companies that provide analytical testing services to support pharmaceutical, biotechnology, and medical device development. They focus on analyzing biological samples, such as blood, plasma, or tissue, to quantify drugs, metabolites, or biomarkers. These services are crucial for preclinical and clinical studies, ensuring accurate and reliable data for regulatory submissions. Bioanalytical CROs help companies save time and resources by offering expertise, advanced instrumentation, and compliance with industry regulations.

What are the key skills and qualifications needed to thrive as a Bioanalytical CRO (Contract Research Organization) professional, and why are they important?

To thrive as a Bioanalytical CRO professional, you need a background in life sciences or chemistry, strong analytical laboratory skills, and often a relevant degree such as a BSc or MSc. Familiarity with technical tools like LC-MS/MS, chromatography software, and compliance with GLP/GCP standards is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These skills ensure accurate data generation, regulatory compliance, and successful execution of client-sponsored research projects.
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What cities are hiring for Bioanalytical Cro jobs? Cities with the most Bioanalytical Cro job openings:
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Bioanalytical Cro jobs near you
Infographic showing various Bioanalytical Cro job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $58,439 per year, or $28.1 per hour.
Senior Scientist, Bioanalytical Sciences

Senior Scientist, Bioanalytical Sciences

CEDENT

Cambridge, MA

$100K - $136K/yr

Full-time

Posted 3 days ago

Job description

The client is seeking an experienced Senior Scientist to join their Bioanalytical Sciences team. In this hands-on, lab-based role, you will lead the design, development, and execution of regulatory-aligned bioanalytical assays supporting IND-enabling studies for our mRNA-LNP therapeutics. You will be a subject matter expert in nucleic acid and protein bioanalysis, working to generate critical data that informs decision-making across preclinical and clinical development. You will be instrumental in building client’s IND readiness and advancing our genetic medicine platform. You will report into the VP, Head of DMPK and Clinical Pharmacology, with the expectation to be onsite 5 days a week. This is an individual contributor role.
You will:
  • Design and execute phase-appropriate bioanalytical strategies for mRNA-based delivery systems
  • Develop, optimize, and qualify RT-qPCR-based assays for quantifying LNP-delivered mRNA in biological matrices
  • Develop and oversee ligand-binding immunoassays (ELISA, MSD, Luminex or similar platforms) for the detection of translated proteins and anti-drug or anti-protein antibodies, including screening, confirmatory, and neutralizing antibody assays in accordance with regulatory guidance
  • Collaborate with stakeholders in DMPK, Toxicology, Clinical, and Regulatory to ensure assay readiness, study support, data integrity, and reporting across GLP and non-GLP studies
  • Become a bioanalytical SME for external CROs to ensure method transfer, scientific rigor, compliance, and execution of assay development, sample analysis, and method validation/qualification
  • Review, interpret, and present bioanalytical data to teams; contribute to the authorship of study reports, assay qualification/validation summaries, and regulatory documentation (e.g., IND Module 4/5)
  • Ensure all analytical work is conducted in alignment with regulatory expectations and fit-for-purpose principles
  • Stay current on emerging technologies and industry standards in nucleic acid and protein bioanalysis.
Qualifications:
  • Ph.D. in Biochemistry, Molecular Biology, Pharmaceutical Sciences, or a related field with a minimum of 5 years of industry experience; an M.S. with 8+ years of relevant industry experience will also be considered
  • Prior contribution to IND submissions or regulatory responses related to bioanalysis
  • Experience with nucleic acid bioanalysis using RT-qPCR for quantifying mRNA or oligonucleotides in preclinical or clinical settings
  • Experience developing and qualifying ligand-binding assays (ELISA, MSD, Luminex) for protein quantification and ADA characterization
  • Experience managing outsourced bioanalytical work, including CRO oversight, protocol review, and data quality control
  • Familiarity with regulatory guidance (e.g., ICH M10) and FDA/EMA expectations for bioanalytical support of IND submissions
  • Experience with data interpretation
  • Commitment to our Core Values: Respect, Integrity, Excellence, and Impact
Cedent logo

About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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