Global Regulatory Jobs in Maidenhead

Job OverviewImplement regulatory strategies & deliverables for a portfolio of products early/late development or marketed products for the Europe Area Regulatory Affairs (ERA) including EU and non-EU countries such as CEE countries Israel Turkey Switzerland and the UK. Include fair representation of...

MAIN PURPOSE OF JOBDefine and implement Area & Affiliate regulatory strategies & deliverables for a portfolio of compounds (early development late development marketed) for the Europe Region.Identify and advocate regions requirements in the overarching global regulatory strategy; develop risk assess...

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 being part of an agile team committed to developing t...

Join Us as a Clinical Trial ManagerWere seeking aClinical Trial Managerto drive the clinical delivery of research trials with precision and purpose. The role will oversee trials in the UK Ireland and the Nordics. If you thrive in a fast-paced collaborative environment and have a passion for clinical...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companies.In this role...

Job OverviewImplement regulatory strategies & deliverables for a portfolio of products early/late development or marketed products for the Europe Area Regulatory Affairs (ERA) including EU and non-EU countries such as CEE countries Israel Turkey Switzerland and the UK. Include fair representation of...

Align with the Director to enhance the roadmap and develop the action plan to implement AbbVies Patient Inclusion strategy across the portfolioCollaborate with cross-functional partners to identify process improvements to disease area strategies and clinical trial lifecycle to increase representativ...

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials (phases I-III) for renowned innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies...

Position Description SummaryActs as the operational interface for both pharmacovigilance (PV) and regulatory affairs teams ensuring platform design delivery and operations support safety compliance and submission needs. This role will focus on optimizing platforms to streamline PV and regulatory pro...

Position Description SummaryActs as the operational interface for both pharmacovigilance (PV) and regulatory affairs teams ensuring technology platform design delivery and operations support safety compliance and submission needs. This role will focus on optimizing platforms to streamline PV and reg...

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 being part of an agile team committed to developing t...