MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Requirements: * BS + in pharmacology, toxicology, biology or chemistry, or related field, with ...
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MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Requirements: * BS + in pharmacology, toxicology, biology or chemistry, or related field, with ...
Quality Assurance Auditor I
Durham, NC · On-site
$70 - $110/hr
S. in chemistry or life sciences or Bachelor's degree or higher in a related field andTwo to four ... As a leading global contract research organization (CRO), we partner with researchers to tackle ...
New
Quality Assurance Auditor I
Durham, NC · On-site
$70 - $110/hr
S. in chemistry or life sciences or Bachelor's degree or higher in a related field andTwo to four ... As a leading global contract research organization (CRO), we partner with researchers to tackle ...
New
Cro Chemistry information
See Raleigh, NC salary details
$13.09 - $14.74
4% of jobs
$14.74 - $16.40
11% of jobs
$17.61 is the 25th percentile. Wages below this are outliers.
$16.40 - $18.06
14% of jobs
$18.06 - $19.71
19% of jobs
The median wage is $19.97 / hr.
$19.71 - $21.37
14% of jobs
$21.37 - $23.03
12% of jobs
$23.25 is the 75th percentile. Wages above this are outliers.
$23.03 - $24.68
12% of jobs
$24.68 - $26.34
3% of jobs
$26.34 - $28
1% of jobs
$28 - $29.66
6% of jobs
$29.66 - $31.31
4% of jobs
$13
$21
$31
How much do cro chemistry jobs pay per hour?
As of Sep 4, 2026, the average hourly pay for cro chemistry in Raleigh, NC is $21.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $23.85 per hour, depending on experience, location, and employer.
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.
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 the difference between Cro Chemistry vs Clinical Research Associate?
| Aspect | Cro Chemistry | Clinical Research Associate |
|---|---|---|
| Required Credentials | Bachelor's degree in chemistry, pharmacy, or related field; often requires industry certifications | Bachelor's degree in life sciences, health sciences, or related; often requires clinical research certifications |
| Work Environment | Laboratories, pharmaceutical companies, research institutions | Clinical trial sites, hospitals, research organizations |
| Industry Usage | Pharmaceutical, biotech, chemical industries | Healthcare, 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 popular job titles related to Cro Chemistry jobs in Raleigh, NC?
For Cro Chemistry jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Cro Chemistry jobs in Raleigh, NC look for?
The top searched job categories for Cro Chemistry jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Cro Chemistry jobs?
Cities near Raleigh, NC with the most Cro Chemistry job openings:
Key responsibilities
Develop, write, and manage highly technical nonclinical documents such as Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure, Nonclinical Study Reports, Meeting Requests, Briefing Documents, and RTQs.
Lead projects independently, ensuring nonclinical submission documents align with regulatory guidelines and meet scientific integrity.
Interpret and analyze pharmacokinetics, pharmacology, and toxicology data to support nonclinical documentation and submissions.
Job description
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position.
Roles and Responsibilities:
- Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, 1st Edition Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs).
- Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical submission documents for INDs/CTAs/NDAs/BLAs/MAAs, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity.
- Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data.
- Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents.
- Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports).
- Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC.
- Demonstrated ability to lead others to complete complex projects.
- Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines.
- Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment.
- Organizational expert within the nonclinical subject area.
- Excellent written/oral communication and strong time and project management skills.
- Ability to attend regular team meetings, lead client meeting and CRMs.
- Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars.
- Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP).
Requirements:
- BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control.
- Knowledge of GLP, ICH guidelines, and applicable regulatory requirements.
- 5+ years of pharmaceutical regulatory nonclinical writing experience.
- Strong writing and analytical skills.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process.
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About M. M. S.
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1 - 10 Employees
Headquarters location
Los Angeles, CA, US
Year founded
1980