Informed Consent Form Specialist - Sponsor Dedicated

**Job Summary**
Under the guidance of Client´s Global Clinical Study Support (“CSS”) management, this position will be responsible for review, coordination and finalization of Global Informed Consent Form templates for all clinical studies that are managed by Development Operations. Responsibilities also include supporting CSS Central Services team as needed.
**Essential Functions**:
- Co-manages maintenance of the centralized Informed Consent Form mailbox.
- Reviews and validates quality and accuracy of Informed Consent Form templates.
- Supports development of Informed Consent Form templates.
- Responsible for tracking progress of Informed Consent Form template language reviews and escalations.
- Edits and reviews Informed Consent Form templates per protocol while ensuring adherence to Incyte standards and study timelines.
- Assist in the reporting of Key Performance Indicators and Central Services metrics.
**Qualifications**
- Bachelor Degree in Health ...

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