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CW
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- $50,000 to $100,000 CAD / year
- Full-time
Are you a results-driven B2B sales professional who enjoys developing new business, building relationships with decision-makers, and closing deals?
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Added 21 mins ago
G
Director, Content Management Team Lead
GSK
Mississauga, ON
- Full-time
…Authority (e.g. FDA, ICH) and internal standards, formats, systems and…
Added 21 mins ago
G
Director, Content Specialist Team Lead
GSK
Mississauga, ON
- Full-time
Strong knowledge of digital content solutions, content automation and content management systems, alongside relevant regulatory requirements.
Added 51 mins ago
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GSK

Director, Content Management Team Lead

Mississauga, ON, Canada

Full-time

Apply on jobs.gsk.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 15, 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.

Position Summary

The Director, Content Management Team Lead is accountable for leading a team of Clinical Content Reviewers and Clinical Content Publishers to ensure submission-ready, high-quality and regulatory-compliant clinical, regulatory and safety content across all therapy areas that supports the successful development and registration of medicines and vaccines.

Leveraging scientific, regulatory and operational expertise, the role will be responsible for building functional capability to execute pipeline deliverables within their remit and embedding innovation.

The role will build effective relationships within the functional leadership, as well as with cross-functional partners across the company and external suppliers to optimize operational delivery of development plans and accelerate cycle times.

Key Responsibilities:

Lead operational delivery ensuring deliverables are of high-quality with adherence to best practices, agreed ways of working and regulatory compliance.
Own resource management planning the effective deployment of internal and external resources to meet portfolio needs in partnership with other Team Leads.
Drive delivery performance by proactively managing dependencies and risks, and resolving complex issues that could impact critical milestones.
Champions continuous improvement by identifying and evaluating potential improvements to practices, as well as leading implementation of enhancements within own area of responsibility assessing effectiveness of the implemented changes.
Advocates for innovation, digital tools and new technologies translating emerging capabilities into practical solutions that enhance team and functional performance.
Develop high-performing teams by guiding people through change, strengthening functional expertise and fostering a collaborative and inclusive culture.

Why you?

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
Experience in end-to-end content quality and publishing operations (electronic submission requirements, technical and regulatory compliance checks, publishing, template management, archival in EDMS and submission delivery), ensuring outputs meet GCP, Health Authority (e.g. FDA, ICH) and internal standards, formats, systems and timelines.
Expertise in contributing to the development and implementation of quality standards, standard operating procedures (SOP)s, creating operational efficiencies through automation.
Broad pharmaceutical, biopharmaceutical or vaccines R&D experience, with strong knowledge of medicines development.

Demonstrated people leadership and talent management experience, including performance management, coaching, talent development, succession planning and capability building.

Strong knowledge of digital content solutions, content automation and content management systems, alongside relevant regulatory requirements.
Strong problem-solving and project management skills, with the ability to manage complex priorities, risks and deliverables.
Excellent written and verbal communication skills in English, with the ability to communicate effectively with senior and cross-functional stakeholders.

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

Advanced degree (Master’s, PhD, PharmD, MD) in a relevant discipline.
Day-to-day fluency in using AI to accelerate trial timelines, improve data quality, evidence assurance, and reduce time spent on manual tasks.
Strong data fluency, including experience using dashboards and performance metrics to drive decisions.

#LI-GSK*

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 Thinking

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.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the Link where you will find answers to multiple questions we receive

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.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Apply on jobs.gsk.com About employer

More about this job

Responsibilities

The Director will lead a team preparing clinical and regulatory submission content, making sure deliverables meet quality and compliance standards. The role plans staffing across internal and external resources, manages risks and improvements, and develops team members.

Requirements

Candidates need a life sciences bachelor's degree, end-to-end regulatory publishing experience and pharmaceutical R&D knowledge. They also need strong people leadership, content management system knowledge and excellent English communication skills.

Skills

Regulatory submissions
Clinical content publishing
EDMS archival
Template management
Content management systems
Content automation
GCP
ICH guidelines
FDA requirements
SOP development
Quality standards
Project management
Risk management
Resource planning
Talent management
Performance management
Coaching
Succession planning
Clinical trial design
Medical writing
Scientific writing
Literature reviews
Dashboards and performance metrics
AI tools

Keywords

Clinical content management
Regulatory submissions
Electronic submission
eCTD
Publishing operations
EDMS
Content management system
GCP
ICH
FDA
SOP
Clinical development
Medical writing
Regulatory affairs
Pharmaceutical R&D
Vaccines
People leadership
Content automation
AI
Project management

Seniority

Lead

Tools

Electronic submission systems
EDMS
Content management systems
Dashboards

Languages

English

Fields of study

Life sciences

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