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Non Clinical Research Jobs in Raleigh, NC (NOW HIRING)

MMS

Senior Nonclinical Writer (US)

Raleigh, NC · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Minimum of 5 years of directly related work experience or equivalent in clinical research, including work on medical device significant risk IDE trials and/or non-significant risk abbreviated IDE ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site

Labcorp is seeking a Sr. Clinical Research Associate - Oncology Evidence Generation to join our ... non-interventional research studies. * Oversee study execution to ensure adherence to protocols ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site +1

Labcorp is seeking a Sr. Clinical Research Associate - Oncology Evidence Generation to join our ... non-interventional research studies. * Oversee study execution to ensure adherence to protocols ...

RemX

Be Seen First

Project Reconciliation Analyst - Clinical Research

Raleigh, NC · Remote

$60K - $70K/yr

Ensure all billable activities and non-visit revenue are properly invoiced and documented ... Clinical Research or Clinical Industry experience is required. * Bachelor's degree. * Minimum of 1 ...

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How much do non clinical research jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for non clinical research in Raleigh, NC is $23.42, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $24.09 per hour, depending on experience, location, and employer.

What is a non clinical research?

A Non Clinical Research job involves conducting studies that do not involve direct testing on human or animal subjects. It includes areas such as data analysis, literature reviews, regulatory research, epidemiological studies, and laboratory-based investigations that focus on drug development, medical devices, or healthcare policies. These roles are essential in shaping clinical trials, ensuring compliance with regulations, and advancing scientific knowledge without direct patient interaction.

What are the typical responsibilities of a non clinical research professional?

Non Clinical Research professionals are responsible for designing studies, collecting and analyzing data, ensuring regulatory compliance, and preparing reports or publications. They often work closely with cross-functional teams, such as project managers, regulatory specialists, and data analysts, to maintain the quality and integrity of research outcomes. Attention to documentation and adherence to industry standards are key parts of the job. By providing structure and oversight to research projects, these professionals help ensure that studies are conducted ethically and produce reliable, actionable results.

What are the key skills and qualifications needed to thrive in non clinical research?

To thrive in Non Clinical Research, you need strong analytical skills, attention to detail, and a background in life sciences or a related field—often supported by a bachelor's or master's degree. Familiarity with research databases, data analysis software (such as SPSS or SAS), and regulatory compliance tools is typically required. Excellent communication, organizational skills, and the ability to collaborate effectively set top candidates apart. These competencies ensure robust, ethical research results and foster productive teamwork in fast-paced research environments.

What are examples of non clinical research jobs?

Non-clinical research jobs include roles such as research coordinators, data analysts, regulatory affairs specialists, project managers, and research assistants. These positions often involve tasks like data management, protocol development, and compliance, typically requiring skills in research methodologies, data analysis tools, and knowledge of regulatory guidelines.

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Non Clinical Research jobs near you
Infographic showing various Non Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $48,709 per year, or $23.4 per hour.

Senior Nonclinical Writer (US)

MMS

Raleigh, NC • On-site

Full-time

Posted 24 days ago

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. 

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

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