Medical Writer I

20 hours ago


Navi Mumbai, India Labcorp Full time

Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs), and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocols and CSRs, and other clinical documents as needed. Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate. Responsible for preparation and review of clinical documents such as patient safety narratives and CSR appendices. Ensure timely delivery of high quality documents to internal customers and Sponsors. Provision of training for Associate Medical Writers and other staff as appropriate. Foster excellent working relationships with all clients, both internal and external, with the highest quality of service in a cost-effective manner on time, every time.

**Labcorp is proud to be an Equal Opportunity Employer**:
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