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Job Details

Principle Medical Writer

Company: Barrington James Medical / Executive
Location:
Reference: PMWCRO4
Closing Date: 10 Dec 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

We have partnered up with a market leading CRO based in the heart of New York City. Due to an influx of new clients, they are looking to expand their Medical Writing function to accommodate for the increased workload going in to 2018.

Requirements:

  • Draft high-quality clinical & regulatory documents that demonstrate a strong grasp of scientific and medical content involved with the drug development process and related clinical trial process (Phase I-III) with excellent understanding of data analysis, data management, and regulatory submissions.
  • Work across departments to help set priorities for document preparation and collaborate on document content.
  • Work with service providers for timely delivery of high quality documents.
  • Write clinical abstracts, clinical study reports (CSR), drug safety update reports (DSUR), IND's, NDA's, posters, and manuscripts.
  • Review and edit clinical and regulatory documents and publications prepared by other authors.
  • Maintain document history and manage version control of documents.
  • Provide guidance for style guides for document preparation.
  • Keep current with relevant therapeutic areas.

Apply for this job: Principle Medical Writer

Contact Information:

Address:  Head Office
Rowan House Smallfield Road Horley Surrey
RH6 9AU
England
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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