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Cro Chemistry Jobs (NOW HIRING)

Analytical Chemist

Chicago, IL · On-site

$65K - $80K/yr

... an award winning, full-service, CRO/Contract Research Organization operating over 25 ... chemistry and manufacturing controls for drug development, and core laboratory services for ...

Production Technician III - CRO, Sr.

Willis, TX · On-site

$16 - $20/hr

... water chemistry, CEMS monitoring and calibrations * Applies skills to perform inspections ... PTECH II - CRO, SR: 2-5 years' experience in a CCGT facility in an Operations or Maintenance ...

Production Technician III - CRO, Sr.

Willis, TX · On-site

$16 - $20/hr

... water chemistry, CEMS monitoring and calibrations * Applies skills to perform inspections ... PTECH II - CRO, SR: 2-5 years' experience in a CCGT facility in an Operations or Maintenance ...

... CRO), or Contract Laboratory Organization (CLO).3+ years of experience working in a regulated GMP ... wet chemistry, glycan analysis, peptide mapping, and physical appearance.Proven ability to lead ...

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

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Cro Chemistry information

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How much do cro chemistry jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for cro chemistry in the United States is $22.26, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $24.52 per hour, depending on experience, location, and employer.

What is the difference between Cro Chemistry vs Clinical Research Associate?

AspectCro ChemistryClinical Research Associate
Required CredentialsBachelor's degree in chemistry, pharmacy, or related field; often requires industry certificationsBachelor's degree in life sciences, health sciences, or related; often requires clinical research certifications
Work EnvironmentLaboratories, pharmaceutical companies, research institutionsClinical trial sites, hospitals, research organizations
Industry UsagePharmaceutical, biotech, chemical industriesHealthcare, pharmaceutical, clinical trial management

Cro Chemistry professionals focus on chemical analysis, formulation, and laboratory research within the pharmaceutical and chemical industries. Clinical Research Associates (CRAs) oversee clinical trials, ensuring compliance and data integrity. While both roles support drug development, Cro Chemistry is lab-based, whereas CRAs work in clinical settings. Understanding these differences helps job seekers identify the right career path in the industry.

What are common challenges faced by professionals in CRO chemistry and how can they be addressed?

Professionals in CRO (Contract Research Organization) Chemistry often encounter challenges such as tight project timelines, shifting client requirements, and the need to quickly adapt to new scientific techniques or technologies. Effective communication with both clients and internal teams is essential to manage expectations and ensure project goals are met. Additionally, strong organizational skills and a proactive approach to problem-solving can help overcome unexpected technical hurdles. Continuous learning and collaboration within multidisciplinary teams also contribute to smoother project execution and personal growth within the field.

What is a CRO chemist?

CRO chemists are professionals who work at Contract Research Organizations (CROs), providing specialized chemical research and development services to pharmaceutical, biotechnology, and other industries. They are involved in tasks such as synthesis, analysis, and characterization of chemical compounds. CRO chemists support drug discovery, process development, and sometimes regulatory submissions, helping clients advance their projects efficiently without expanding in-house capabilities. Their expertise allows companies to access advanced chemistry services on a contract basis, saving both time and resources.

What skills and qualifications are needed to thrive as a CRO chemist?

To thrive as a CRO Chemist, a solid background in organic and analytical chemistry, supported by a degree in chemistry or related fields, is essential. Familiarity with laboratory instrumentation such as HPLC, GC-MS, NMR, and proficiency in using LIMS or ELN systems are typically required, along with any relevant safety or GLP certifications. Strong attention to detail, problem-solving skills, and effective teamwork enable chemists to deliver accurate results on client-driven projects. These competencies ensure high-quality research, regulatory compliance, and successful collaboration within contract research organizations.
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Cities with the most Cro Chemistry job openings:

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States with the most job openings for Cro Chemistry jobs include:

Infographic showing various Cro Chemistry job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $46,292 per year, or $22.3 per hour.

Director, Analytical Chemistry

Moderna Therapeutics

Cambridge, MA

Full-time

Medical, PTO

Re-posted 18 days ago


Moderna rating

9.2

Company rating: 9.2 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

5th of 86 rated pharmaceutical


Job description

The Role:

Moderna is seeking a Director, Analytical Chemistry to provide scientific, strategic, and organizational leadership for discovery-stage analytical chemistry activities supporting mRNA-lipid nanoparticle (LNP) research across a diverse portfolio of nucleic acid medicines. This leader will define and advance analytical strategies that enable rapid design-make-test-learn cycles across novel ionizable lipids, polymers, excipients, payloads, formulations, and delivery systems used in mRNA-LNP therapeutics and vaccines.

The successful candidate will serve as a senior analytical partner to medicinal chemistry, computational chemistry, formulation, delivery sciences, platform biology, and selected development functions to accelerate molecular design, analytical decision-making, and candidate progression. The individual will guide analytical approaches spanning small molecules, polymers and lipid characterization, impurity profiling, structure elucidation, orthogonal physicochemical characterization, and fit-for-purpose evaluation of RNA, lipid, and nanoparticle attributes in support of discovery and early development objectives.

Building Moderna's technical model for analytical leadership, this role will provide strategic oversight of method development, method qualification and transfer where appropriate, characterization, impurity identification, and analytical control strategy concepts relevant to discovery and translational research. The leader will help define decision-quality analytical packages, ensure alignment of analytical deliverables with program milestones, and provide technical guidance and oversight to both internal teams and external CRO/CDMO partners.

This position requires deep expertise in modern analytical chemistry and a strong ability to translate complex data into actionable scientific decisions. The ideal candidate will combine technical depth in separation science, characterization, and structure elucidation with proven leadership experience, sound scientific judgment, and the ability to build productive partnerships across internal teams and external collaborators. Experience supporting transitions from discovery through IND-enabling or early clinical development is strongly valued. Experience with high-throughput methodologies is highly desirable, and familiarity with artificial intelligence and machine learning techniques is considered a strong plus.

This role will be in Cambridge, MA.

Here's What You'll Do

  • Lead and develop a high-performing team of analytical scientists and, depending on organizational design, matrix-lead additional scientists across analytical chemistry, characterization, and platform functions supporting discovery-stage mRNA-LNP research.

  • Set the analytical chemistry vision and strategy for discovery-stage mRNA-LNP programs, ensuring fit-for-purpose analytical capabilities are available to support lipid design, payload evaluation, formulation screening, and candidate advancement.

  • Serve as the senior analytical partner to medicinal chemistry teams by enabling structure confirmation, purity and impurity profiling, route support, reference standard strategy, and rapid troubleshooting for novel lipids and related small molecules.

  • Partner closely with computational chemistry and data science teams to translate molecular design hypotheses into analytical learning plans, generate data sets that improve structure-property understanding, and inform iterative design of ionizable lipids and related delivery materials.

  • Collaborate with formulation and delivery sciences teams to establish robust analytical workflows for screening and characterizing LNP systems, including support for lipid composition assessment, encapsulation-related analytics, degradation pathways, and physicochemical attribute characterization.

  • Guide fit-for-purpose analytical method development, optimization, qualification, transfer, and lifecycle management across chromatography, mass spectrometry, spectroscopy, and orthogonal characterization platforms.

  • Provide scientific leadership in small molecule and lipid structure elucidation, impurity identification, forced degradation or stress studies where relevant, and root-cause analysis of analytical or material quality issues.

  • Oversee analytical characterization strategies for relevant large molecules and nucleic acid components, with familiarity in mRNA or related RNA analytics and the interfaces between drug substance, formulation, and drug product performance.

  • Work with discovery, platform, and selected development teams to ensure analytical deliverables, technical risk assessments, and timelines remain aligned with program objectives and portfolio milestones.

  • Provide technical leadership and oversight to external partners, including CROs and CDMOs, for specialty characterization, method transfer, development support, and data package review.

  • Author and review technical reports, analytical development documentation, invention disclosures, publications, and selected regulatory-facing analytical content as appropriate for the maturity of the program.

  • Serve as a strategic and technical partner to Research, Technical Development, Analytical Development, and Process Chemistry and Development functions to drive analytical strategy discussions, define action items, and build scalable capabilities where discovery and development intersect.

  • Represent analytical chemistry in cross-functional governance, portfolio discussions, technical reviews, and external interactions, and help shape investment priorities for instrumentation, digital workflows, and scientific capability building.

  • You will apply high-throughput methodologies to accelerate research and development efforts, leveraging artificial intelligence and machine learning techniques to enhance data analysis and decision-making.

  • Analytical development in Moderna is structured around a centers-of-emphasis model and accordingly the individual will liaise with the appropriate teams and groups to lead technical and strategic efforts in the area of small molecule, lipid, RNA, and nanoparticle analytics.

Here's What You'll Need (Basic Qualifications)

  • Ph.D. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, Chemical Biology, Chemical Engineering, or a closely related discipline, with 9+ years of relevant industry experience; a strong M.S. candidate with significant leadership experience may also be considered.

  • Substantial experience in analytical chemistry supporting discovery research and/or early development in biotech or pharmaceutical settings, including demonstrated leadership at the program, function, or platform level.

  • Deep expertise in small molecules, polymers and lipid analytical chemistry, including structure elucidation, impurity assessment, method development, advanced characterization, and the use of orthogonal analytical approaches and tools for novel chemical entities or excipients.

  • Deep expertise in separation techniques and analytical platforms such as UPLC, HPLC, LC-MS, LC-CAD, GC-MS, CE, NMR, UV/Vis, IR, particle or colloidal characterization methods, and other relevant physicochemical and spectroscopic techniques.

  • Working knowledge of large molecule and nucleic acid analytics, with meaningful familiarity in mRNA or related RNA characterization and an understanding of how RNA quality attributes interface with formulation and delivery performance.

  • Demonstrated managerial abilities and strong technical leadership in both direct reporting relationships and in a matrix and cross-functional environment to execute strategy.

  • Experience with technology transfer to internal or external partners and with building productive working relationships with CRO and/or CDMO collaborators.

  • Experience in developing phase-appropriate analytical strategies and control concepts in settings that bridge discovery and development, including familiarity with technical documentation that supports progression into regulated environments.

  • Sound understanding of analytical methods pertaining to mRNA-LNP products and their components, including the relationships between lipid identity, composition, formulation properties, and product performance.

  • Familiarity with electronic laboratory notebooks, CDS, LES, and/or LIMS and an interest in modern data workflows that improve decision making and execution speed.

  • Experience applying high-throughput methodologies to accelerate research and development, along with proficiency in leveraging artificial intelligence and machine learning to enhance data analysis and inform decision-making.

  • Excellent communication and influence skills, with the ability to distill complex analytical data into clear recommendations for senior leaders and diverse scientific stakeholders.

  • Exceptional ability to drive teams toward best practices in a fast-paced environment while helping build durable technical and business processes.

  • This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.

Here's What You'll Bring to the Table (Preferred Qualifications)

  • Experience supporting mRNA-LNP, oligonucleotide, gene editing, or related nucleic acid modalities in discovery, translational, or early development settings.

  • Experience with lipid library characterization, ionizable lipid structure-property relationships, and analytical support for high-throughput or iterative formulation screening workflows.

  • Experience contributing to IND-enabling or early clinical development programs, including analytical sections of technical reports, regulatory submissions, or health authority responses.

  • Familiarity with design-of-experiments, multivariate data analysis, cheminformatics-enabled workflows, and digital laboratory systems.

  • Experience with high-throughput methodologies is highly desirable, and familiarity with artificial intelligence and machine learning techniques.

  • A publication, patent, or innovation record that demonstrates scientific thought leadership in analytical chemistry, delivery sciences, or nucleic acid therapeutics.

  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.

  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs

  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support

  • Family planning benefits, including fertility, adoption, and surrogacy support

  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown

  • Savings and investment opportunities to help you plan for the future

  • Location-specific perks and extras

The salary range for this role is $167,000.00 - $300,700.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Our Working Model

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

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About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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