[Next-Generation Sequencing Book]
  • [Photo] Marilyn Delacruz • May 21, 2003
    Our client currently has several positions open for Medical Writers in the Southern NJ area.

    Responsibilities include:
    • Writing sections of Clinical Trial Reports, NDAs or other regulatory summary documents, and a variety of other clinical research related documents.
    • Identifying and organizing materials, and interpreting data in preparing the above-referenced documents.
    • Additionally, assisting in establishing the format and content of the above-referenced documents, ensuring adherence to regulatory guidelines.
    Qualifications:
    • BS/BA in Life Sciences required.
    • Minimum 2 years experience in scientific environment, in a pharmaceutical or CRO environment necessary.
    • Medical writing experience and familiarity with ICH-compliant study reports necessary.
    • Experience must include data handling and analysis.
    • Excellent written and verbal communication skills and ability to work independently.
    • Word processing skills necessary.
    Please contact Valerie Voon at 800-862-2330 or via email at valerie.voon[at]comrise.com.

    [Please reference Bioinformatics.Org when replying to this announcement.]

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