The Role This a portfolio-level regulatory strategy role covering regions with diverse regulatory requirements and market dynamics: APAC, LATAM, MEA, CIS, Adriatics and Partner Business Regions. Working with the Therapeutic Area Lead, youll set regional regulatory
The role Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is to be office based in central London for at least 3 days a week
Overview Alnylam Pharmaceuticals is seeking an imaginative physician drug developer. This is an opportunity to provide clinical leadership in developing RNAi therapeutics in Alnylam’s rapidly expanding portfolio, which spans the areas of rare genetic diseases, cardio‑metabolic
Head of Global Labelling CSL Seqirus influenza vaccine portfolio reaches millions of people every year, and every product depends on labelling that is scientifically sound, regulatory compliant, and clear and informative for the end‑user. This position
We are excited to be recruiting for a Director of Public Affairs to support the UK, responsible for developing and executing strategic communications plans, creative campaigns and other initiatives that deliver high-impact results focused on driving
Job Description The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables
An innovative biopharmaceutical organisation is seeking an experienced Associate Director within Safety Surveillance and Aggregate Reporting to provide scientific and strategic leadership across global pharmacovigilance activities. Key Responsibilities Lead safety surveillance activities for assigned products. Oversee
CSL R&D is driving significant transformation — accelerating its data and AI ambitions in a way that demands architecture thinking rooted in business value, not just technical delivery. The R&D Data Architect is a brand new
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means
Head of Global Labelling The Role CSL Seqirus influenza vaccine portfolio reaches millions of people every year, and every one of those products depends on labelling thats scientifically sound, regulatory compliant, and is clear and informative
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Value & Access Lead Temporary 3 month contract Maidenhead/Remote £(Apply online only) per day SRG are partnering with a global pharmaceutical company who have a new opening for a Market Access Lead to join them on
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
CSL Seqirus in Maidenhead is seeking a Regional Regulatory Lead to shape regional strategies across APAC, LATAM, MEA, CIS, Adriatics and Partner Business. You will oversee submissions, life-cycle management and health authority relationships, translating global strategy
Regional Regulatory Lead - APAC, LATAM, MEA, CIS, Adriatics and Partner Business Location: Maidenhead/Hybrid, 3-days a week on-site The Role This a portfolio-level regulatory strategy role covering regions with diverse regulatory requirements and market dynamics: APAC,
The Role This a portfolio-level regulatory strategy role covering regions with diverse regulatory requirements and market dynamics: APAC, LATAM, MEA, CIS, Adriatics and Partner Business Regions. Working with the Therapeutic Area Lead, youll set regional regulatory
We are excited to be recruiting for a Director of Public Affairs to support the UK, responsible for developing and executing strategic communications plans, creative campaigns and other initiatives that deliver high-impact results focused on driving