Principal Medical Writer

Global biopharmaceutical company is seeking a Principal Medical Writer inWarren,New Jerseyto be engaged in submission document writing, leading regulatory writing efforts, and being an integral part of the tight-knit writing team. This is a brand new position that has opened up due to the heavy expansion of the drug pipeline. Responsibilities: - Management of medical writing projects, regulatory documents, timelines, and key document writing - Write phase I-IV clinical and regulatory documents and submissions, including IBs, CSRs, integrated summaries of efficacy and safety, clinical overviews, protocols, registration dossiers, package inserts, briefing books, and responses to health authorities -Lead submissions and manage, train, mentor, and work closely with other writers Requirements: -5+ years of solid medical writing experience -BS required, advanced degrees such as MS or PhD desirable -Experience in immunology and inflammation is a plus, but not required -Highly capable team player with strong interpersonal skills -Leadership initiative, ability to multi-task and complete assignments on time Do not miss this opportunity to get your dream medical writing job as a principal writer in a stable, financially strong international pharmaceutical company! Apply today and send resumes to Jess Lakis at Real Pharma; reach me at 212-707-8499.

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com/en/