Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents
Location: United Kingdom (Home-Based) Contract Type: Freelance FTE: 1.0 Start: Immediate Duration: Approximately 3–6 months About the Role We are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Location: Home-based, UK or Sweden At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission
ICF is seeking a senior aviation technical adviser to strengthen our aircraft leasing and technical advisory capability. The role is suited to an experienced aviation professional with deep knowledge of aircraft assets, lease structures, maintenance obligations, technical
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Company: Ultra Intelligence & CommunicationsMarconi Technologies/Communications Business Powering Decision Join the team redefining defense technology. From engineering systems that save lives to leading programs that change the battlefield—find your place in the future of defense. Communications
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage clinical research projects in different therapeutic
Company: Ultra Intelligence & CommunicationsMarconi Technologies/Communications Business Powering Decision Join the team redefining defense technology. From engineering systems that save lives to leading programs that change the battlefield—find your place in the future of defense. Communications
Job Title: Local Study Associate Director Location: United Kingdom Introduction to role: Are you ready to lead country-level study delivery that accelerates breakthrough cancer therapies to patients? This role places you at the heart of pivotal
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Who We Are BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered
Description For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents
Your mission Contribute to the execution of gene therapy and associated projects per development plan, from planning and initiation through to closeout. Ensure that all clinical study management and project deliverables are completed on time, within
Reporting to: VP Pharmacovigilance Location: London, UK / Hybrid Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative, potentially curative
Reading, Berkshire, United Kingdom Full time R To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international
Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents in
Location: UK-wide (remote/hybrid as applicable). Please note that this role can be based anywhere within the UK.Who were looking forWe are looking for a Lead Consultant (Economist) to join ICFs growing economics function within our UK Policy