(India)
About Us Kateric is a strategic partner for biopharmaceutical companies that consistently delivers superior quality regulatory documents through excellence, experience, and intelligent execution. Kateric\xe2\x80\x99s resources are located across multiple time zones in the United States, as well as in India, the EU and Canada, and also have experience working with client teams located across the globe. About the Role We currently have opportunities for Indian medical writers to author safety documents for pharmaceuticals. Our writers are responsible for driving the development of each deliverable including de novo writing (to varying levels) and/or managing stakeholder contributions, ensuring adherence to client styles and formatting, managing stakeholder expectations, and ensuring timeline integrity across a wide variety of document types (e.g., Development Safety Update Reports, PSURs, PBRERs, RMPs etc.). We provide the training, tools, infrastructure, and support needed for our writers to be successful. We also provide significant development opportunities for our team members resulting in exposure to a wide variety of document/product types and therapy areas. Flexibility to work some evening hours to accommodate global client meetings. Pre-screen interview and proctored writing assessment are screening requirement as part of the recruiting process. Additional Responsibilities
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