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... Northeast Id : 24965 Technical Writer - Med Device Contract 6 ... installation guides for future company medical devices and medical software systems. Coordinating with internal ... Coordinating with..
EXTERNAL POSTING TITLE
Scientist I, Cell line engineering and genome editing
Biogen is seeking a highly motivated molecular and cell biologist to join the Assay and Screening Technologies group ..
The Claims Editor enhances the Hospital's revenue by reducing claim edit denials resulting from charge entry and/or coding errors and omissions. The Claims Editor works closely with the Claims Edit Coordinator ..
Are you ready to join an organization where you can make an
Imagine all Americans enjoying ideal cardiovascular health free of heart disease and stroke. At the ..
Science Writer/Editor in Boston Massachusetts Since its ... patient care. The Department of Medical Oncology seeks a Scientific Writer and Editor to assist various ... assist various members of the..
Administrative Associate II
Title Administrative Associate II
Job Posting Description At Boston Children’s Hospital, success is measured in patients treated, parents comforted and teams taught. It’s ..
Understanding of the clinical and drug development process
Prior experience in hemophilia preferred but not essential
Understanding of the writing and review process for each document type
Understanding of applicable ..
... next few years.. Remote based Medical Writer for Clinical and R and ... the Clinical Operations Team on medical writing deliverables. To provide advice ... deliverables. To provide advice..
... and technology advanced. In major medical breakthroughs and small acts of ... the teaching hospital of Harvard Medical School, our reach is global ... Join our acclaimed Department of..
The Senior Medical Writing Scientist is responsible for ... of regulatory submissions. The Senior Medical Writing Scientist may assist other ... Writing Scientist may assist other Medical Writing staff to..
nThe full-time Senior Medical Writer Contractor will prepare clinical/regulatory documentation (protocols, study reports, sections of NDA/MAA in CTD format, publications, etc.) to support successful submissions in the US, EU, and rest ..