Vice President, Global Regulatory Affairs Strategy - Wavre

GSK is seeking a Vice President for Global Regulatory Affairs Strategy to oversee regulatory strategy globally for the RI&I portfolio. The role will involve ensuring appropriate regulatory compliance in the conduct of global development programs and product lifecycle maintenance. ...

GSK has bold ambitions for patients aiming to positively impact the health of 25 billion people by the end of decade Our R D focuses on discovering and delivering vaccines medicines combining our understanding of immune system with cutting edge technology to transform peoples liv ...

+Job Summary · In this critical leadership role · , you will oversee regulatory strategy globally for GSK's RI & I portfolio. · +Responsibilities · Directly accountable for global regulatory development and filings for RI&I portfolio products.Ensures sound regulatory practices ar ...

In a context of constantly evolving health policies at the Belgian, European, and international levels AbbVie is seeking a Government Affairs Manager to lead its advocacy strategy for the Belgium–Luxembourg affiliate. · ...

Provide hands-on medical execution support to the BeLux Respiratory & Specialty Medical Affairs, ensuring compliant, high-quality delivery of medical content, training, and activities for biologics portfolio. · ...

Głównym celem jest kształtowanie zewnętrznego środowiska dla naszych leków poprzez pracę nad polityką regulacyjną w Europie i na świecie. · Wydajemy się przede wszystkim do rozwoju priorytetów i strategii w zakresie regulacji farmaceutycznych oraz budowania relacji z organami nad ...

The Medical Science Liaison position at GSK involves building advocacy for vaccination strategies in Belgium through scientific partnerships with External Experts and Scientific Associations. · ...

We are seeking a skilled Medical Affairs professional to provide hands-on support to our Respiratory & Specialty Medical Affairs team. · Medical/scientific review of promotional & non-promotional materials; guarantee compliance & local regulations. · Distil complex data into clea ...

Are you energized by building advocacy for vaccination strategies in Belgium through the development of a scientific partnerships with key External Experts and Scientific Associations? · ...

We are looking for professionals with these required skills to achieve our goals: · Higher degree in life sciences: PhD, MSc or equivalent, · A significant (e.g. 2 years) amount of pharmaceutical industry experience in a role successfully engaging in scientific exchange with exte ...

We are building an exceptional team and pipeline of potentially leading products like MINIject to establish new treatment paradigms in eye care conditions with the highest patient needs. · Lead end‑to‑end management of international ophthalmology trials (FIH, pivotal, PMCF). · Ov ...

We are seeking an experienced and dynamic Executive Director, Strategic Labelling to lead global labelling development and governance for GSK's diverse portfolio of medicines and vaccines. · ...

Lorem ipsum dolor sit amet. · Develop and maintain Europe/EU regulatory policy · ...

This role will play a pivotal part in ensuring global promotional content meets highest standards of quality,sientific accuracy,balance,and compliance. · ...

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

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 stand ...

This role will play a pivotal part in ensuring global promotional and non-promotional content meets high standards of quality. The Associate Director Content Approval for Vaccines will foster robust relationships within Commercial Legal Medical Affairs Regulatory Affairs Clinical ...

Site Name: UK – London – New Oxford Street, Belgium-Wavre, Durham Blackwell Street, Philadelphia Walnut Street, Upper Providence · Posted Date: Mar 9 2026 · As an Associate Director, Content Approval for Vaccines, you will play a pivotal role in ensuring the global promotional an ...

The Director of Europe Regulatory Policy leads regulatory policy work that shapes the external environment for our medicines. · ...

The Vaccines Clinical Sciences Cluster Head is responsible for ensuring the delivery of robust Clinical Development Plans (CDPs) that explore new areas of interest and alternative development pathways. · Accountable for clinical development planning of assets within their disease ...