Regulatory Documents Jobs in Kent W

Job Description SummaryAs a Senior* 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 Senior/Clinical Development Medical Director (CDMD) is the clinical leader of...

You will lead medical writing activities that support clinical development and regulatory submissions. You will work closely with clinical pharmacology non-clinical pre-clinical research regulatory biostatistics and/or external partners to plan author and deliver complex documents. We value clear sc...

Were here for one reason and one reason only to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. Weve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we...

DescriptionJob title: Regulatory Affairs Specialist- Graduate Apprentice x2Department: Regulatory AffairsLocation: Fareham Hampshire (moving to the Vision Centre Southampton in September 2026)GLS: P02Working hours: Monday Friday 8:30 to 4:30 (3 days office based/ 2 remote)A brighter future awaits y...

POSITION SUMMARYYou will provide clinical and scientific oversight and support for multiple global Phase 1 - 4 clinical studies in support of the development strategy for programs within the Vaccines portfolio.POSITION RESPONSIBILITIESMaintains current scientific and clinical knowledge in the specif...

DescriptionPlease note we have a separate job advert for candidates interested in joining our Medical Communications teams which you can find here: Costello Medical - Current Openings. Please apply for one role at a time because assessment processes differ.Role Summary Responsibilities: You will wor...

DescriptionPlease note we have a separate job advert for candidates interested in joining our Medical Communications teams which you can find here: Costello Medical - Current Openings. Please apply for one role at a time because assessment processes differ.Role Summary Responsibilities: You will wor...

Job Description SummaryThe Senior* Clinical Development Medical Director (Sr* CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As Senior/CDMD in the Renal TA you will have oversight of the...

DescriptionPlease note we have a separate job advert for candidates interested in joining our Value and Access or Evidence Development teams which you can find here: Costello Medical - Current Openings. Please apply for one role at a time because assessment processes differ. Role Summary Responsibil...

We create a place where people can grow be their best be safe and feel welcome valued and included. We offer a competitive salary an annual bonus based on company performance healthcare and wellbeing programmes pension plan membership and shares and savings programme.We embrace modern work practises...

Make your mark for patientsWe are looking for a Principal Scientist Non-Clinical PKPD who is innovative and agile to join us in our Clinical Development Sciences Group based at the R&D site in Slough UK then Windlesham Surrey (2027).About the role The Non-Clinical PKPD group sits within the Quantita...

Title:Senior Medical WriterCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs...

A Career with PurposeBionical Emas is a global Early Access Programs (EAP) and Clinical Trial Supply (CTS) group bringing life-changing medicines to patients around the world. Their range of services and capabilities benefit many of the worlds leading pharma and biotech companies.At Bionical Emas yo...