- Expiry Date: 07 July 2022
- Referral: email@example.com
The Technical Writer for Clinical Trial Capabilities Data Standards is responsible for developing the company's Standards for innovative clinical trial capabilities, such as econsent, ePRO, telemedicine, etc.
The data standards will create minimum requirements and a consistent approach for these novel capabilities that aren't yet broadly incorporated into the company's ways of working and procedural documents.
Work with the GDD Innovation Program Leadership Team and identified Business Capability Owners to develop Data Standards
Works with Business Capability Owners to acquire thorough knowledge of the capabilities for content documentation that is being developed
Assess available information across other areas to determine whether any existing standards can be utilized and revised or new documents need to be created.
From assessment take available information and develop draft of data standards to be used for Business Capability Owner and SME review.
BA/BS degree or equivalent in a relevant scientific discipline as well as medical or computer science background.
5+ years of direct experience in content development, communications and technology documentation in Pharma industry.
Excellent writer and editor.
Familiar with and have experience in the Pharma industry and the clinical development capabilities/processes.
Ability to translate complex ideas and information into organized, guided documents.
Understanding of content creation best practices (capture, creation and organization of information across multiple channels).
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