Regulatory Documents Jobs in UK

Job Description SummaryLOCATION: London or Homeworker Dublin Barcelona ROLE TYPE: Hybrid Working #LI-HybridThe Clinical Development Medical Director (CDMD) is the Global clinical leader of defined and assigned program level activities and deliverables (e.g. submission activities briefing books etc.)...

Job Description SummaryLOCATION: London Dublin Barcelona ROLE TYPE: Hybrid Working #LI-HybridThe Associate Clinical Development Director (Assoc. CDD) provides input to development of protocols for assigned global clinical trials scientific monitoring and reporting of quality data. May be assigned to...

Work Location:London United KingdomHours:35Line of Business:TD SecuritiesPay Details:Were committed to providing fair and equitable compensation to all our colleagues. As a candidate we encourage you to have an open dialogue with a member of our HR Team and ask compensation related questions includi...

Work Location:London United KingdomHours:35Line of Business:TD SecuritiesPay Details:Were committed to providing fair and equitable compensation to all our colleagues. As a candidate we encourage you to have an open dialogue with a member of our HR Team and ask compensation related questions includi...

CK Group are recruiting for a Principal Scientist PKPD to join a global pharmaceutical company on a contract basis initially for 12 months. Salary: 35.20 Per hour (PAYE) / 47.92 (Umbrella) - flexible for experienced candidates. Principal Scientist PKPD Role:Participate in the development of non-cl...

CK Group are recruiting for a Regulatory Affairs Associate to join a leading global food brand company on a contract basis until December 2026. This is a hybrid role with 2 days per week in Reading. Salary: From 25 ph PAYE Regulatory Affairs Associate Role:Support and maintain pharmaceutical product...

The Scientist for Clinical Trials - Oncology - Thoracic (Sr. Manager) (non-MD) is responsible for providing support of scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.Job Responsibilitie...

Full time. Remote in the UK Spain Portugal or Greece.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Principal Medical Writer to lead authoring and development of high complexity clinical regulator...

Sponsor-dedicated. Full time. Remote in the UK Greece Spain or Portugal.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and development of high co...

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...

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...

Regulatory Affairs Specialist (Full-time Permanent)Hybrid - AylesfordUnlock your potential with PrinovaWe are Prinova a leading global supplier of ingredients and premix manufacturing solutions and trusted by the worlds best-known food beverage and nutrition brands.Part of the NAGASE Group our exper...

Senior Manager Regulatory Compliance If youre looking for a career that will help you stand out join HSBC and fulfil your potential - whether you want a career that could take you to the top or an exciting new direction we offer opportunities support and rewards that will take you further.Were one o...

This is an opportunity to join the Environment Agency and their Permitting Service. The role is a great way to develop into other roles and career paths within the Agency.Our Permitting Support Team needs enthusiastic individuals to manage incoming license and permit applications providing support t...

Title: Regulatory Reporting ManagerContract Type: PermanentLocation: BradfordWorking Pattern:Hybrid (usually a couple of days a week in the office). We welcome part-time and flexible arrangements and will aim to match your current flexibility where We OfferWe care about your wellbeing not just your...

Job Description SummaryAs a Clinical Development Medical Director you will be responsible for the scientific and clinical strategy of assigned clinical trials scientific monitoring and reporting of quality data.The Clinical Development Medical Director (CDMD) is the clinical leader of defined progra...

Director Vaccine Clinical Research and Development (MD)ROLE SUMMARYPrimary purpose is to serve as a Clinician within a Pfizer vaccine development program. This role may serve as a clinical lead for one or more studies within a clinical program and works closely with the global clinical program lead...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Director Oncology Translational Research Liaison ScienceJob PurposeThe Director Oncology Translational Research Liaison Science will play a key role in the Oncology Translational Research (OTR) team within GSK Oncology. The post holder will exploit GSK proprietary and internally generated datasets f...