Senior Medical Writer

MediVector is looking for a highly motivated and skilled Medical Writer, preferably with experience in Infectious Disease.  The ideal candidate will be responsible for writing a variety of documents, including protocols, informed consents, clinical trial reports, etc., related to our ongoing development programs.

 Responsibilities:

• Prepare, edit, and review all clinical documents (e.g., study protocols, Investigator's Brochures, study reports and documents for IND/NDA applications), and abstracts, posters and articles.
• Ensure compliance to FDA reporting requirements, quality, and resource requirements.
• Review/edit documents for organization, clarity, grammar, language and scientific standards; and resolve errors and inconsistencies in clinical data with biostatisticians and other project team members.

Qualifications:

The successful candidate will have:

• A graduate degree preferred and 5+ years’ experience in medical writing for a biopharmaceutical company or relevant organization
• Excellent Microsoft Office skills with an emphasis on Word
• Clearly demonstrated ability to write high-quality documents
• Ability to independently analyze and synthesize data
• Demonstrated ability to manage multiple projects from conception to completion in a fast-paced setting
• Demonstrated ability to function as a  team player who relates well internally and externally

Qualified candidates should submit resume with cover letter to James L. McEvoy at:  jmcevoy@medivector.com