IQVIA Technical Writer – Compliance Products in New Brunswick, United States
The technical writer will be responsible for working with the product management, development, and QA teams to develop all material all associated with a new product or an existing product release. The individual will require heavy interaction with the Business Analysts to understand final functionality and design. Interactions will also be required with client implementation teams to address and rectify feedback for each CCOE product. The deliverables will include product manuals, user/training guides, and release notes with a focus on the new GTM product suite. The initial requirement of this role will be to lay out the vision and a plan to scrub all legacy material and define a path and strategy forward. Once the plan is finalized with the Product Management Director the individual will be responsible for executing that plan and reporting status to the entire CCOE organization with support from the Product Management Director and/or the various product managers and owners for the products within CCOE. The role will directly manage 1 business analyst based in the US.
The candidate will require daily interaction with the product management team and client implementation teams located in NY/NJ.
The individual must be fluent in all aspects of Healthcare Compliance. Transparency and HCP/HCO interaction is a plus.
The individual will be responsible for 5-7 products each consisting of 7-10 deliverables with 2-3 major releases per year and 1-2 minor releases per year. Each release for each product requires publication of associated materials.
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IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
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