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    Company: Novartis Healthcare

    Location: Hyderabad, AP

    Date Posted: April 07, 2013

    : To support and/or lead activities related to reconciling, writing, editing and/or managing the production of high quality clinical documentation (e.g. Clinical Study Reports and Summary Documents) for submission to regulatory authorities in support of marketing applications. Desired Profile: PhD in Life Sciences/Applied Biology MD in Internal Medicine/ Pharmacology MBBS, MPharm, MSc by Research Additional Requirements: Publications in indexed journals/ high quality scientific writing, including previous writing experience in safety documents (including narratives) and clinical study reports (CSRs) Relevant experience (at least 2-3 years) in leading pharmaceutical/research companies, including medico-marketing, or academic/research institutions Disease/Therapeutic area expertise...

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    from FirstSalary.com - 30+ days ago