Senior Nonclinical Writer (Remote - Canada)

mmsholdingsinc; Toronto; Remote; CAD 90,000 - 120,000; Full time

Job summary

MMS Holdings Inc. seeks a seasoned regulatory writer to join our remote team, focusing on development and management of highly technical nonclinical documents for regulatory submissions.

You will lead writing projects, interpret GLP and nonclinical study data, and collaborate with cross-functional teams to ensure scientific integrity and regulatory compliance across submissions.

Qualifications

• BS in pharmacology, toxicology, biology or chemistry or related field
• Knowledge of GLP, ICH guidelines and 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 drug development terminology

Responsibilities

• Develop and write nonclinical submission documents (Module 2.4/2.6 eCTD, IB, Nonclinical Study Reports)
• Lead projects independently, writing nonclinical submission documents for INDs/CTAs/NDAs/BLAs/MAAs
• Author based on GLP and nonclinical study data
• Develop mapping plan for placement of nonclinical studies in Module 2.4/2.6
• Interpret and analyze PK/TOX data (e.g., PK/TK evaluation reports)
• Collaborate with cross-functional teams (PM, safety, efficacy, biostats, regulatory ops, CMC)
• Lead others to complete complex projects
• Ensure documents follow sponsor format and regulatory guidelines
• Negotiate, persuade, collaborate, and use analytical judgment
• Be organizationally expert in nonclinical subject area
• Exhibit excellent written/oral communication and time/project management
• Attend team meetings, lead client meetings and CRMs
• Work in client systems (SharePoint, Veeva RIM, PleaseReview, EndNote) and templates
• Strong understanding of regulatory guidances (ICH, FDA/EMA, GLP, GCP, GMP, GDP)

Skills

Writing skills

Analytical skills

Regulatory interpretation

Communication (oral/written)

Education

Bachelor degree in pharmacology/toxicology/biology/chemistry

Tools

MS Office

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,1stEditionInvestigator’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 nonclinicalsubmissiondocumentsfor 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.

Please consider your application unsuccessful if we do not reach out to you within 14days of your submission.