Nonclinical Writer

Nonclinical Writer – MMS

Join to apply for the Nonclinical Writer role at MMS
. This is a full-time remote position.

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) that prides itself 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 a proven, scientific approach to complex trial data and regulatory submission challenges.

With a global footprint across four continents, MMS maintains an industry‑leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive.

Visit  or follow MMS on Linked In for more exciting opportunities and why MMS is a great place to advance your career.

• Strong experience with development and writing of nonclinical documents (e.g., Module 2.4 and 2.6 eCTD submission documents, 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 documents, ensuring the package aligns with current regulatory guidelines and meets scientific integrity
• Author documents based on highly technical sources such as GLP and non‑GLP nonclinical study reports, in vivo and in vitro nonclinical data
• Develop a mapping plan for the placement of nonclinical studies within the structure of Module 2.4 and 2.6 eCTD submission documents
• Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (e.g., 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
• Complete documents according to sponsor’s format, processes, and regulatory guidelines
• Effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
• Excel as an organizational expert within the nonclinical subject area
• Possess excellent written/oral communication and strong time and project management skills
• Attend regular team meetings, lead client meetings and CRMs
• Work in various client systems (e.g., SharePoint, Veeva RIM, Please Review, End Note), templates and toolbars
• Strong understanding of regulatory guidances as they apply to nonclinical submission documents and drug development (e.g., ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)

• BS+ in pharmacology, toxicology, biology, chemistry, or a related field, with industry experience in regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
• Knowledge of GLP, ICH guidelines, and applicable regulatory requirements
• 2+ 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, and the drug development process

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