In this role you will
- Lead the development and execution of regional regulatory strategy for assigned assets, aligned with global strategy and regional requirements.
- Act as the single point of contact for regional regulatory, ensuring alignment across Global Regulatory Leads (GRLs), local regulatory teams, and cross‑functional stakeholders.
- Provide regulatory expertise and market insight to anticipate risks, identify opportunities, and support decision‑making.
- Drive delivery of submissions and approvals, ensuring timely, compliant execution across the region.
- Collaborate with global and local teams to integrate regional requirements into development plans, including clinical, GMP, and submission strategies.
- Ensure clear communication of regulatory plans, milestones, risks, and strategic implications to stakeholders.
- Support continuous improvement, innovation, and knowledge sharing across regulatory teams.
Basic Qualifications & Skills
- Bachelor's Degree in Biological or Healthcare Science.
- Strong experience in regional regulatory strategy, submissions, and approvals.
- Knowledge of clinical development, regulatory requirements, and agency processes.
- Ability to work cross‑functionally and influence stakeholders in a matrix environment.
- Strong decision‑making and problem‑solving skills with ability to assess regulatory impact.
- Proven ability to manage complexity, anticipate risks, and drive solutions.
- Digital fluency and ability to leverage tools to enhance delivery and efficiency.
Preferred Qualifications & Skills
- PhD in Biological or Healthcare Science.
- Experience of all phases of the drug development process in regulatory affairs.
Benefits
We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
Equal Opportunity Employer
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.
#J-18808-Ljbffr”, “datePosted”: “2026-05-19”, “hiringOrganization”: { “@type”: “Organization”, “name”: “GlaxoSmithKline”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__435991526__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=33” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “London” } } }In this role you will
- Lead the development and execution of regional regulatory strategy for assigned assets, aligned with global strategy and regional requirements.
- Act as the single point of contact for regional regulatory, ensuring alignment across Global Regulatory Leads (GRLs), local regulatory teams, and cross‑functional stakeholders.
- Provide regulatory expertise and market insight to anticipate risks, identify opportunities, and support decision‑making.
- Drive delivery of submissions and approvals, ensuring timely, compliant execution across the region.
- Collaborate with global and local teams to integrate regional requirements into development plans, including clinical, GMP, and submission strategies.
- Ensure clear communication of regulatory plans, milestones, risks, and strategic implications to stakeholders.
- Support continuous improvement, innovation, and knowledge sharing across regulatory teams.
Basic Qualifications & Skills
- Bachelor’s Degree in Biological or Healthcare Science.
- Strong experience in regional regulatory strategy, submissions, and approvals.
- Knowledge of clinical development, regulatory requirements, and agency processes.
- Ability to work cross‑functionally and influence stakeholders in a matrix environment.
- Strong decision‑making and problem‑solving skills with ability to assess regulatory impact.
- Proven ability to manage complexity, anticipate risks, and drive solutions.
- Digital fluency and ability to leverage tools to enhance delivery and efficiency.
Preferred Qualifications & Skills
- PhD in Biological or Healthcare Science.
- Experience of all phases of the drug development process in regulatory affairs.
Benefits
We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
Equal Opportunity Employer
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.
#J-18808-Ljbffr…