Director, Content Design and Delivery Scientific Communications, Vaccines

il y a 2 semaines


Wavre, Belgique GSK Temps plein

**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK - London, USA - Maryland - Rockville, USA - North Carolina - Durham
**Posted Date**: Jul 25 2025

The** Director, Content Design and Delivery Scientific Communications, Vaccines in the Global Scientific Communications organization**is responsible for chairing Global Integrated Medical Communication Teams (GIMCT) for the Vaccines asset/disease area and driving the development of Integrated Medical Communication Plans (IMCP). This includes the creation of content, channel, and congress plans/tactics, ensuring the timely execution of deliverables such as the Scientific Communication Platform (SCP), Scientific Narrative, content and channel plans, and associated congress tactics.

This role will ensure the delivery of scientifically accurate, evidence-based, and compliant materials for healthcare professionals, patients, and internal teams.

**Key Responsibilities**:

- This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following._
- Chair the Global Integrated Medical Communication Teams (GIMCT) for assigned assets/therapeutic areas to drive the development of Integrated Medical Communication Plans (IMCP), inclusive of content, channel, and congress plans/tactics.
- Drive key asset deliverables including the Scientific Communication Platform (SCP), Scientific Narratives, Content and Channel plans, Congress Plans and all associated tactics.
- Serve as a key partner to therapeutic area medical leaders, global publications, R&D, Global Medical Team (GMT), and priority markets and regions.
- Collaborate with internal stakeholders on the development and execution of innovative tools for internal and external communication, including digital/social medical delivery.
- Drive timely execution of all deliverables within the IMCPs for assigned assets, ensuring they are scientifically accurate, evidence-based, and comply with relevant regulations, industry guidelines, and ethical standards.
- Accountable for aligning with key stakeholders and for the input of the IMCP framework and related engagement planning elements within the asset annual business planning process.
- Lead annual scope of work development with procurement for IMCP deliverables with agencies of record, and provide continuous oversight and feedback to drive effective collaboration and partnership
- Ensure content development follows all relevant codes and system requirements (e.g. ABPI code of practice, GSK Code, and use of Content Lab), particularly with respect to the delivery of promotional versus non-promotional information.
- Participate in initiatives on Gen AI platforms being leveraged for content creation and personalization/adaptation to ensure broader scalability and use
- Gather and share best practices across Global to ensure consistency, high standards, and excellence are maintained across the organization.
- Stay updated on advancements in scientific communications to ensure content approaches evolve with the external landscape.

**Basic Qualifications**:

- We are looking for professionals with these required skills to achieve our goals:_
- Advanced Life Sciences degree in science, medicine, or pharmacy is required.
- 7 or more years of related experience in scientific communications, medical content design and delivery, within the pharmaceutical or healthcare industry.
- Experience in leading cross-functional teams and driving strategic end to end communication plans.
- Develop and execute innovative communication tools, including digital and social media strategies.
- Project management skills with the ability to manage multiple projects.
- Experience in developing and delivering medical training materials and presentations to HCPs and senior leadership.
- Experience in digital content creation and management tools with solid technical capabilities in Excel, PowerPoint, and Team sites.

**Preferred Qualifications**:

- If you have the following characteristics, it would be a plus:_
- Postgraduate degree (PhD or PharmD).
- Local, regional, or global medical or R&D experience with relevant expertise in Vaccines therapeutic area.
- Scientific communication strategies for large global markets in US, UK, EU, China and Japan.
- Ability to interpret, analyze, organize, and present complex data to a broad range of audiences.

LI-GSK

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

**Why GSK?**

**Uniting science, technology and talent to get ahead of disease together.**

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and ge



  • Wavre, Belgique GSK Temps plein

    As an Associate Director, Content Approval for Vaccines, you will play a pivotal role in ensuring the global promotional and non-promotional content meets the highest standards of quality, scientific accuracy, balance, and compliance. This includes adherence to internal GSK standards and applicable external regulations, including a robust understanding of...


  • Wavre, Belgique GSK Temps plein

    Job Purpose:The Global Medical Director role is designed for an experienced, innovative, and proactive medical professional who is passionate about advancing the understanding of the value of our medicines and vaccines. You will develop and implement global medical scientific strategies to generate insights, shape optimal care through scientific dialogue and...


  • Wavre, Belgique GSK Temps plein

    Job PurposeThe Senior Global Medical Affairs Director role is a unique opportunity for an experienced, innovative, and proactive medical affairs professional to provide strategic medical affairs enterprise leadership within Global Therapeutic Areas (TAs) at GSK. You will play a pivotal role in setting and delivering the long-term disease and medicine...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: UK - London - New Oxford Street, Belgium-Wavre, Canada - Ontario - Mississauga - Milverton Drive, Poznan Grunwaldzka **Posted Date**: Jun 9 2025 As a Senior Manager, Regulatory Communication Lead you will be responsible for developing and executing a comprehensive communication strategy across Global Regulatory Affairs (GRA) organisation,...


  • Wavre, Belgique GSK Temps plein

    Job PurposeThe Senior Global Medical Affairs Director role is a unique opportunity for an experienced, innovative, and proactive medical affairs professional to provide strategic leadership within GSK’s Global Therapeutic Areas (TAs). You will play a pivotal role in setting and delivering the long-term disease and medicine strategy for a key portfolio or...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: UK - Hertfordshire - Stevenage, Mississauga, Warsaw, Wavre **Posted Date**: Feb 18 2025 **Job Purpose**: GSK’s success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where...


  • Wavre, Belgique Proclinical Temps plein

    Proclinical are working alongside a pharmaceutical corporation who are recruiting for an individual to join their team. This role is on a permanent basis. The opening position is for a Director - Clinical Assay Platform Lead. For more information, please get in touch now! **Responsibilities**: - Guide the consistent increase in performance allowing to...


  • Wavre, Belgique GSK Temps plein

    Business IntroductionAt 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...


  • Wavre, Belgique SGS Temps plein

    Description de l'entreprise SGS est une importante société internationale d’inspection, de vérification, de testing et de certification. La société emploie plus de 97 000 personnes et dispose d’un réseau de plus de 2600 bureaux et laboratoires dans le monde. **Afin de rejoindre notre laboratoire de SGS Lab Simon à Wavre, nous sommes actuellement...

  • Director privacy R&D and CPO

    il y a 2 semaines


    Wavre, Belgique GSK Temps plein

    Director, Privacy R&D and CPOJob PurposeA Director Privacy for R&D/CPO ensures compliance with global data protection laws like GDPR and HIPAA. They mitigate privacy risks and safeguard sensitive health data to ensure patient privacy right are respected and right avoid legal and reputational damage. The role fosters study participants trust by ensuring...