Clinical SOP Writer

Location: Cambridge, Massachusetts, United States
Salary: negotiable
Job Type: Contract
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The Clinical Standard Operating Procedures (SOP) Writer is responsible for working with Subject Matter Experts (SMEs) to prepare new or changes to existing clinical Policies, SOPs, and Work Instructions as part of an overall document harmonization and integration project. The Clinical SOP Writer is responsible for implementing the document workflow process as a formal written procedure. The Clinical SOP Writer is also responsible for supporting the development and revision of procedures by applying document standards, criteria and adhering to timelines.

Responsibilities and Requirements:

Supports the full clinical procedure lifecycle for Policies, SOPs, Work Instructions (WIs) and Forms by serving as a SOP Writer Works with author and SMEs on to implement agreed up on procedures development applying appropriate document standards and criteria, ensuring terminology consistency across documents. Collects input from stakeholders and consolidates comments, resolving conflicts collaboratively Translates process maps or other process representations and applies them to SOP procedures wording Contributes to the development and maintenance of up-to-date Clinical SOP Writer procedures so that the process is used and consistently applied by all Clinical SOP Writers Maintains tracking spreadsheets and timelines, as assigned Performs other duties, as assigned Displays the ability to manage customer expectations Demonstrates proactive thinking and actions Familiar with cross-functional customer service techniques Ability to multi-task in a fast-moving environment.

If you or someone you know feel this could be an opportunity you would like to explore please send me your most up to date resume at c.hesler (at sign) to discuss the role in further detail.

Sthree US is acting as an Employment Business in relation to this vacancy.

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