Empleos de icf en Murcia

One of our client is continuing its digital transformation programme to improve the effectiveness, coherence, and transparency of its online communication activities. The programme supports the development and operation of large-scale web platforms and collaborative digital solutions used by a broad range of stakeholders. A specialised digital services team...

Senior Medical Writer/Principal Medical Writer Remote, Spain 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...

ICF International is recruiting a Junior User Support & Web Operations Specialist to support hosting, deployment, and maintenance of Drupal-based web platforms. You will work with developers, project teams, and stakeholders to ensure smooth operation and continuous improvement of web solutions. The role emphasizes deployment activities, incident handling,...

Premier Research is looking for a Senior Regulatory Submissions Lead to join our Regulatory Submissions and Contracts team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we...

Premier Research is looking for a Senior Regulatory Submissions Lead to join our Regulatory Submissions and Contracts team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we...

Senior Medical Writer/Principal Medical Writer Remote, Spain 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...

** Please submit your application in English ** What You'll Do:Support of Regulatory Affairs Study Start-Up (RASSU) department: * Assist/Advise project teams on all regulatory requirements for clinical studies * Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings *...

Senior Medical Writer/Principal Medical Writer Remote, Spain 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....

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 compliance with Precision MW Style Guide, Precision...

Premier Research is looking for a Senior Regulatory Submissions Lead to join our Regulatory Submissions and Contracts team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics.What we do is profoundly connected to saving and improving lives, and we...

Position SummaryThe 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 compliance with Precision MW Style Guide, Precision...