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Transversal Finance Lead
Sanofi
Toronto, ON
- Full-time
Added 12 mins ago
SJ
Senior Customer Service Representative
SC Johnson
Brantford, ON · CAN - Brantford
- Full-time
…to participate in this recruitment process, please contact Human…
Added 12 mins ago
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Supervisor, Front of House (LBE)
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- Part-time
Execute all company programs and service standards on an ongoing basis and provide feedback to the employees and Service Manager to improve the Guest service experience.
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Fisheries Populations Monitoring and Regulations Manager - State Prog Admin Manager Sr
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Assistant Manager, Guest Experience | Contract August 2026 - June 2027 | Royalty Crossing Pop Up, PEI
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GSK

Principal Medical Writer

Mississauga, ON, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 1, 2026

Original job description

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D

Position Summary

The Principal Medical Writer is a seasoned expert who owns complex safety writing deliverables end-to-end. In this role, they independently lead the authoring of high-impact safety documents - such as aggregate reports and Risk Management Plans (RMPs) - translating complex safety data and analyses into clear, compelling outputs. They are accountable for driving timelines, managing stakeholders, and ensuring the quality of safety deliverables that address important safety issues. Beyond day-to-day delivery, this role is a key champion for continuous improvement, best practices, and the smart adoption of new tools and technologies in the safety writing space.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Independently lead preparation of complex clinical and post-market safety documents (e.g., DSURs, PSURs/PBRERs, ACOs, PADERs/PAERs, RMPs, and responses to regulatory authority questions), with strong hands-on experience across all key aggregate safety documents.
Operate effectively within a global, complex matrix organization, working autonomously and confidently influencing stakeholders on process discipline, quality standards, and “how” work should be done.
Lead cross-functional teams to develop content strategy, coordinate contributions, manage review schedules and timelines, and ensure high-quality, fit-for-purpose documents that accurately reflect safety, clinical, and statistical data and meet GSK and global/regional/local regulatory requirements.
Provide oversight to co-authors, vendor writers, and teams of writers - serving as a mentor/buddy, ensuring the quality of contributions, and leading initiatives to improve medical writing processes, including effective use of authoring/review tools and other automation/AI-enabled technology platforms.

Why You?

This role is hybrid. You will work on-site in Canada part of the week and remotely the remainder. Exact on-site days will be agreed with your manager.

Basic Qualifications
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

Bachelor’s degree in life sciences, health sciences, pharmacy, nursing or a related field.
Minimum 5 years of advanced medical/regulatory safety writing experience in pharmaceutical, biotech or clinical research settings, including summarization and interpretation of complex data and independent preparation of complex clinical and safety documents for regulatory use.
Advanced understanding of, and ability to apply, statistical, regulatory and medical communication concepts needed to independently write complex safety documents.
In-depth working knowledge of relevant regulatory guidance (e.g., ICH, GVP, FDA, EMA) pertaining to clinical trial conduct, pharmacovigilance, and document-specific requirements, as well as Good Clinical Practice (GCP).
Strong understanding of core cross-functional clinical research roles and procedures (e.g., safety, regulatory, clinical, epidemiology, statistics and programming) and how they relate to document strategy and operational preparation.
Experience across multiple therapeutic areas, with confidence to quickly dive into new areas without extensive lead time.
Proven ability to manage multiple projects and deadlines in a fast-paced, global/matrix environment, working autonomously while effectively influencing stakeholders.
Strong written and verbal English communication skills and excellent attention to detail.

Preferred Qualifications
If you have the following characteristics, it would be a plus

Advanced degree (PhD, PharmD, MSc, MPH) or equivalent scientific training.
Advanced safety writing skills with expertise across most key safety document types and experience leading regulatory submission projects or preparing dossier modules.
Comfort interpreting statistical outputs and collaborating with statisticians on tables and data displays.
Highly collaborative and capable of leading cross-functional, multicultural, and hybrid/distributed teams across regions - negotiating solutions, advising on document structure and content, and working effectively with diverse stakeholders (e.g., health authorities, external partners, contractors/CROs, and patients).
Experience working with external partners, contractors or clinical research organizations, including vendor oversight and coordination.
Prior mentoring, training or people development experience, supporting the growth of less experienced writers and team members.
Able to independently lead multiple projects simultaneously and deliver multiple high-quality documents on schedule.
Advanced computer skills and general computer literacy, including comfort with collaboration tools and remote-working technologies.
Excellent English language proficiency, both verbal and written.

What you will gain
You will join a team focused on patient impact and continuous learning. You will develop technical and strategic skills in regulatory writing, submission planning and cross-functional collaboration. Your work will shape development programs and contribute to better outcomes for patients.

Ready to apply?
If this role fits your skills and ambition, we want to hear from you. Please apply and tell us how your experience will help shape treatments that matter.

Skills

Clinical Development, Clinical Trial Designs, Communication, Customer Service, Decision Making, Emotional Intelligence, Influencing Without Authority, Learning Agility, Literature Reviews, Medical Writing, Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions, Scientific Writing, Strategic ThinkingIn compliance with Ontario's provincial pay transparency legislation, this job posting includes a salary range to support equitable and informed hiring practices. The annual compensation for this role is CAD118,000 to CAD168,000 , determined based on experience, qualifications, and internal equity. GSK is dedicated to promoting transparency and fairness throughout our recruitment process.Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at canada-recruitment@gsk.com. Please do not send resumes to this e-mail and instead apply through the online application process of this posting.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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More about this job

Responsibilities

The Principal Medical Writer leads the end-to-end authoring of complex safety documents such as aggregate reports and Risk Management Plans. They also manage cross-functional teams, drive content strategy, and provide mentorship to ensure high-quality regulatory deliverables.

Requirements

Candidates must hold a bachelor's degree in a life sciences field and possess at least 5 years of advanced medical or regulatory safety writing experience. A deep understanding of global regulatory guidance, clinical research procedures, and the ability to interpret complex safety data are essential.

Skills

Medical Writing
Regulatory Writing
Pharmacovigilance
Clinical Research
Risk Management Plans
Aggregate Reports
Data Analysis
Regulatory Guidance
Project Management
Stakeholder Management
Cross-functional Leadership
Mentoring
Quality Assurance
Regulatory Submissions
Scientific Writing
Strategic Thinking

Visa sponsorship

Not detected in the job text

Keywords

Medical Writing
Pharmacovigilance
Regulatory Affairs
DSUR
PSUR
PBRER
RMP
Clinical Trials
ICH
GVP
FDA
EMA
GCP
Life Sciences
Biotech
Pharmaceutical
Data Interpretation
Regulatory Submissions
Cross-functional Collaboration
Vendor Oversight
Automation
AI-enabled Technology
Safety Data
Epidemiology
Statistics
Regulatory Compliance
Document Strategy
Matrix Organization
Mentorship
Quality Standards

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