REGULATORY AND CLINICAL PROJECT jobs in United Kingdom #3

, or Germany. Responsibilities: – Write and/or edit various clinical regulatory documents: As a Senior Regulatory Affairs... Writer, you will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs...

advice to project teams to ensure continued regulatory compliance and timely market release. Support external regulatory...CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry...

environment. Responsibilities: Support the team in ensuring regulatory requirements are met for Clinical Trial Applications... Affiliate. Provide regulatory advice to project teams to ensure continued regulatory compliance and timely market release...

that regulatory requirements are met for Clinical Trial Applications that involve Medical Devices of any nature (e.g. physical devices... regulatory advice to project teams to ensure continued regulatory compliance and timely market release. Support external...

We have an opportunity for a Senior Regulatory Manager within the Clinical Development team. You will be a highly skilled and experienced... regulatory expert, with recent hands-on experience of successful clinical trial submissions within the Latin America and/or Asia...

understanding of Clinical Trials, submissions process and overall Life Science Industry Regulatory environment. In this role...: Manage the team of Regulatory Affairs (Pharma, Medical Devices, Clinical Trials…) and ensure that projects are delivered...

approval, regulatory affairs, drug development consultancy, and post approval/marketing support. We are known for our hands...-on problem-solving approach and enjoy tackling the unique challenges that each project brings. Our clients span the...

in clinical studies. You will provide operational and technical regulatory assistance through all stages of clinical... regulatory input during clinical development to ensure compliance of diagnostics used in therapeutic trials with global and local...

Specialist are to; Liaise with Corin Ltd R&D and Product Management to provide regulatory input into NPI Project Core teams.... Experience in medical device/orthopaedics regulatory affairs, ideally Class 3 is essential Experience in clinical evaluation...

teams; ability to broadly represent the regulatory functions on project teams within BMS and across alliance. Experience... clinical trials in communicating between Diagnostic sponsor and Drug sponsor. Experience as a member of Global Regulatory sub...

, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical...Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK Join us on our exciting journey! Remote...

a pivotal role in leading and coordinating clinical nursing practice, education, research, and consultation within our Clinical... Community Care division, ensuring high quality evidence based clinical care underpins all actions and interactions with the...

-functional teams including R&D personnel (clinical operations teams), quality assurance/quality control (QA/QC) teams, regulatory... UK homecare market, providing clinical patient care directly to over 50,000 people in their own community...

awareness. Vendor management experience. Familiarity with medical terms, Good Clinical Practice, and regulatory guidelines...Salary: £380 - £400 per hour Job type: Contract * Discipline: Project/Study Manager (CSM/CPM) * Location: United...

, inspection readiness, etc. Support program team Ensures that the clinical sections of regulatory documents (Investigator..., clinical pharmacology, commercial, regulatory, outcomes research, Global Product Development and other members of the extended...

Job Description Position Description: Senior Specialist, Clinical Literature Monitoring Provides pertinent... and timely information on our Company’s products and interests from the world’s biomedical literature in support of regulatory...

awareness of the regulatory issues and requirements surrounding clinical trials and research studies Experience of working...Owlstone Medical Ltd is on a mission to save 100,000 lives. To achieve this, within Clinical Study Delivery we support...