Nonclinical Writer

MMS; Bridgeport (CT); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Supportive and innovative team

Recognized for exceptional culture

Great Place to Work certified organization

Job summary

A clinical research organization is seeking a Nonclinical Writer to develop and manage nonclinical documents for regulatory submissions. This role requires strong writing skills, 2+ years of experience in regulatory writing, and the ability to collaborate effectively with different teams. The position is full-time and remote, suitable for those with a background in pharmacology or related fields.

Qualifications

• 2+ years of pharmaceutical regulatory nonclinical writing experience.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Basic understanding of CROs and scientific & nonclinical data.

Responsibilities

• Develop, write, and manage highly technical nonclinical documents.
• Lead projects independently with minimal oversight.
• Collaborate with cross-functional teams.

Skills

Regulatory writing

Strong writing and analytical skills

Knowledge of GLP and ICH guidelines

Excellent communication skills

Time management

Education

BS+ in pharmacology, toxicology, biology or chemistry

Tools

MS Office applications

SharePoint

Veeva RIM

PleaseReview

EndNote

Job description

Join to apply for the Nonclinical Writer role at MMS. 3 weeks ago Be among the first 25 applicants.

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 an 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, 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, 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 meetings 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
• 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, & the drug development process