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Publié hier

Director, Content Management Team Lead

@ GlaxoSmithKline Services Unlimited

Télétravail au Canada

TélétravailTemps plein
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En bref

GlaxoSmithKline Services Unlimited is hiring a Director, Content Management Team Lead to lead a team of clinical content reviewers and publishers. The role ensures submission-ready, regulatory-compliant clinical, regulatory and safety content for medicines and vaccine development. The posting states a full-time position with an agile working culture where flexibility can be discussed.

Responsabilités :

  • Lead operational delivery of high-quality clinical content
  • Manage internal and external resource planning
  • Drive delivery performance and manage risks and dependencies
  • Champion continuous improvement and innovation
  • Develop high-performing teams

Résumé des exigences :

  • Bachelor's degree in life sciences
  • End-to-end content quality and publishing experience
  • Pharmaceutical or vaccines R&D experience
  • People leadership and talent management experience
  • Knowledge of digital content solutions and content management systems
  • Excellent English communication skills

Outils et compétences

Source et dates

Site carrière / système de candidatures · workday

Date publiée par l’employeur
2026-11-12
Première détection par notre source
2026-11-13
Mise à jour du dossier source
2026-11-13

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauDirecteur ou directrice
DomaineOpérations
Gestion d’équipeOui
Heures par semaine40 (estimé)
Milieu de travailBureau
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
FormationBaccalauréat (exigé), Maîtrise (préféré)
Domaines d’étudesLife sciences

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

GlaxoSmithKline Services Unlimited

ChampValeur
Offres sur Jobsy5
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 QualificationIf 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 [email protected] 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/

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