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Principal Regulatory Medical Writer
£50,000 - £58,000 per annum
LONDON
...Study Reports (CSRs), Investigator's Brochures (IBs) and other clinical/scientific reports within the Cancer Research UK CDD. You'll provide specialist guidance and advice to others and promote best practice in medical writing, including identifying improvements and ensuring consistency. You'll...
Senior Project Clinical Data Manager
, , UNITED KINGDOM
Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London. The company have a strong leadership team who are accelerating growth and have a great vision for the future. The offices are very modern and they have a fully kitted out clinical...
Start up Line Manager London
LONDON, ENGLAND, UNITED KINGDOM
...cross-functional project teams globally for the assigned studies in start up phase Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. Monitor study timelines, patient recruitment, budget at Start up phase Participate in bid...
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Senior Project Clinical Data Manager
UNITED KINGDOM, UNITED KINGDOM
p b Senior Project Clinical Data Manager /b /p p br /p p We have the pleasure of working with a fantastic early phase CRO based in London. The company have a strong leadership team who are accelerating growth and have a great vision for the future. The offices are very modern and they have a...
Senior Medical Director - CNS/Neurology - Europe - Home-based
LONDON, ENGLAND, UNITED KINGDOM
...team support the larger project team and help establish the scientific and medical expertise that characterizes the philosophy here at Worldwide. Activities include direct interactions and presentations with medical and operational personnel from pharmaceutical companies in the process of business...
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HSE Manager
DONCASTER
...and governance to the project on all health and safety related subjects. What you' ll be doingImplementation of the HSES strategy for the business Lead and manage the overall capability, development, deployment and performance of health and safety requirements...
Associate Clinical Project Manager
, , UNITED KINGDOM
...an Associate Clinical Project Manager on a permanent full-time capacity. Purpose of the Role: The Associate Project Manager will support the Project Management Team and contribute to the successful delivery of IXICO s clinical trials, research studies and collaborations under the guidance and...
Clinical Project Manager (Remote)
, , UNITED KINGDOM
Clinical Project Manager / Senior Clinical Project Manager As a Clinical Project Manager, you will become part of a team working for and reporting to the Head of Clinical Operations. You will have primary responsibility for the set-up and management of several clinical studies within the clinical...
Clinical Project Director
, , UNITED KINGDOM
RRxCo is partnered with a clinical-stage Biotechnology Company that develops novel medicines for severe immune disorders. This exciting and innovative firm is expanding its team by creating an opening for a Clinical Project Director. Focused on the field of auto-immune disorders, our client is set...
Laboratory Scientist
, , UNITED KINGDOM
...the needs of research projects. The data you will produce will contribute to scientific discoveries which will support the creation of new or improved products and services that reach millions of pets across the world through our brands to make a better world for pets. Being part of the WALTHAM...
Medical Science Liaison (Inflammation)
, , UNITED KINGDOM
...Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Global Medical, Global Clinical and external partners Ensures high standard of professionalism to develop and...
Environmental Team Lead
, , UNITED KINGDOM
...including projects, drilling, infill, etc. The role will report directly to our QSSHE Manager and will be based in Norwich working Monday to Friday. There may be some required travel to other sites and on occasions visits offshore. Key Responsibilities Include: Management of all...
Principal Consultant, Clinical
, , UNITED KINGDOM
...preparation of project proposals & educational materials, review written estimates, quotations and contracts for Clients as required Contribute to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Clinical and Drug Development Plans...
Principal Scientist: Pharmacometrics
ALDERLEY EDGE, ENGLAND, UNITED KINGDOM
...whole portfolio). as project leader for client projects, providing strategic and scientific PK/PD and biopharmaceutics advice across all stages of discovery and clinical development. to the design, analysis, and interpretation of non-clinical and clinical pharmacology studies. human PK and dose...
International Heritage Program Manager
, , UNITED KINGDOM
Company Profile Chronicle Heritage International is a premier heritage management-only consulting firm with a track record of completing large-scale archaeological projects in the United States and the Kingdom of Saudi Arabia (KSA). The group succeeds by combining the thorough knowledge of...
Senior Intelligence Analyst
, , UNITED KINGDOM
...their progression and project delivery. Supporting client engagement, interaction and presenting intelligence back to clients. On day one you will bring: Experience in online research, digital investigations, open-source intelligence (OSINT). Experience of mentoring, training, or managing...
Senior Clinical Trial Manager
, , UNITED KINGDOM
...including protocol, investigator brochure, informed consent, etc. Participate in Case Report Form design and user acceptance testing in partnership with Data Management as well as data monitoring over the course of the study. Oversee study management and/or clinical development teams (CROs) to...
Clinical Study Lead (maternity leave)
UNITED KINGDOM, , UNITED KINGDOM
...including protocols, investigator brochure, informed consent, contracts, and reports, in compliance with relevant regulations, guidelines and SOPs. The Trial Lead is responsible for creating and implementing study-specific clinical monitoring tools and documents responsible for managing and...
Health & Safety Specialist
SWINDON, ENGLAND, UNITED KINGDOM
...Stakeholder and project management Flexible to adapt to the demands of an ever-changing business environment Able to think strategically and is solution focused Adaptable A strong understanding and proven execution of existing Health and Safety processes and procedures Proven ability in...
Medical Director
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
...clinical trials. Lead project teams in the design and implementation of clinical studies, ensuring adherence to quality standards and timelines. Draft protocols, investigator brochures, and clinical study reports, while also reviewing trial documents. Facilitate investigator meetings and site...
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