Medical Writer - Regulatory Affairs and Clinical Trials

Our client is a rapidly growing small pharmaceutical company with many drugs in various stages of development for indications such as CNS, Immunology, Cardiovascular disease, Oncology, Asthma, Diabetes. This dynamic pharma is looking for an experienced Medical Writer.

This position is responsible, with very minimal supervision, for the preparation of a variety of documents supporting all phases of drug development including, study protocols, abstracts, study reports (all phases), IND and NDA sections, annual reports.

The Medical Writer will also manage the document distribution, review and approval process, coordinate and conduct document review meetings and interface with all departments involved with drug development ensuring that all documents are of high quality, scientifically accurate and in compliance with company and regulatory requirements. There will be some flexibility to work from home a few times/month.

The ideal candidate for this position will have a Bachelors Degree in a Scientific Discipline, Advanced degree desirable. Must have at least three years of directly related pharmaceutical sector experience, especially IND and NDA filing. The individual must also be able to work in a team or on his/her own whenever necessary.

In return for your loyalty and hard work, our client offers a very competitive salary, great benefits and a truly wonderful working environment. This is a permanent full time position on site in our client's Northern New Jersey Headquarters.  Interested/Qualified candidates, please send your current CV/Resume in MS Word format to Caryn Reiman, caryn@ultimatesolutions.com or call 201-909-3717 for more information