Medical WriterJobs In

Bethesda,MD

Position will be an integral part of the client organization implementing European Medical Devices Regulation MDR for disposable and electromechanical devices A candidate will be responsible for re

Rockville,MD

Were seeking a highly motivated selfdriven and enthusiastic Regulatory Affairs writer to join our Regulatory Affairs Team At RemeGen our regulatory affairs group is responsible for drafting and re

Gaithersburg,MD

MMS is an awardwinning datafocused CRO that supports the pharmaceutical and biotech industries with a proven scientific approach to complex trial data and regulatory submission challenges Strong

Rockville,MD

This position will lead the medical writing activities for multiple programs within Clinical Research Individual will be reviewingwriting clinical documents in support of Phase 14 clinical studies

Seattle,WA

King Of Prussia,PA

Des Plaines,IL

Seattle,WA

This position will report to the Senior Director Medical Writing and will be based in Vancouver BC or Seattle WA Key Responsibilities Leads development and authoring of programlevel and study

Santa Clara,CA

Position Overview The Sr Medical Writer is responsible for the development and creation of highquality scientific communications materials for presentation and publication in scientific peer

Hillsboro,OR

Medical Writer The Medical Writer conducts literature and clinical data searches writes and evaluates medical and scientific content and manages clinical evaluation reports and their process to

South San Francisco,CA

The Principal Medical Writer will be responsible for authoring and revising clinical and regulatory documents for submission to the FDA and other agencies and may also lead other internal and

Seattle,WA

This position will report to the Senior Director Medical Writing and will be based in Vancouver BC or Seattle WA Key Responsibilities Leads development and authoring of programlevel and study

Menlo Park,CA

Manage medical writing timelines for assigned documents to ensure ontime deliverables that meet business needs Facilitate comment resolution with authors reviewers and project teams May

Alameda,CA

Prior medical technical writing experience within the biotechpharmaceuticalCRO realm Experience and significant participation in preparation of clinical documents for regulatory submissions eg

Coquille,OR

Director Medical Writing Reports to Head of Clinical Operations Overview Of Position Reporting to the Head of Clinical Operations the Director Medical Writing is responsible for providing

San Francisco,CA

The DirectorAssociate Director Medical Writing is responsible for leading clinical regulatory medical writing activities that conform to domestic andor international regulatory submission This

San Francisco,CA

or medical device sector Minimum of 5 years of technical writing experience Experience in using a Document Management Systems as a Technical Writer Proficient with configuration change

San Francisco,CA

Technical Writer Remote 6 month Contract Seeking Senior Technical Writer for 6 Month Contract Job Title Senior Technical Writer Job Location 100 Remote Requirements 8 years as a

San Francisco,CA

REMOTE UX CONTENT WRITER We are currently seeking a UX Content Writer for a 9 month possiblemedical condition genetic information mental and physical disability political affiliation

Milpitas,CA

Senior Technical Writer Location Milpitas CA 95035 Duration 12 Months Job Description 8 to 10 years of experience for developing User Manual and Quick Start Guides for Protocol Analyzer