Regulatory Writer - 1 Full-time Job

Regulatory Writer - 1

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Job Overview Acts as a MedTech Medical Writer on more advanced writing projects, more challenging initiatives or customers. Prepares assigned MedTech documents including clinical/performance evaluations, evaluation reports, post market surveillance plans and reports for either internal customers or external clients. Documents may be related to medical devices, combination products and in-vitro diagnostics (IVD) with content consistent to industry regulations and client specifications.

Builds strong, lasting relationships with internal colleagues and client teams.

Prepares assigned documents in accordance with IQVIA MedTech Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Negotiates timelines and discusses/resolves client comments. Provides written and verbal feedback to clients when appropriate.