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Senior Editor, Consent Form Development
AdvarraSupports IRB Services by reviewing incoming submissions and editing informed consent forms. Collaborates with stakeholders to ensure regulatory compliance in human subjects research.
About the role
Key responsibilities & impact- Supports the IRB Services department in the review of incoming submissions and preparation of informed consent forms (ICFs) used in the conduct of human subjects research
- Conduct an accurate pre-review of new and revised consent forms in regulatory compliance
- Edit new and revised consent forms to ensure regulatory compliance and alignment with Advarra operational standards
- Collaborate with Board members and staff to include all necessary edits to the consent form from the various stakeholders
- Mentor new team members, as requested
- Maintain and increase individual regulatory knowledge to assist with organizational compliance
Requirements
What you’ll need- Minimum of 2 years of experience in technical/medical writing and/or editing
- Experience writing and/or editing consent forms or other research documents
- Proficiency in Word processing and editing (including use of Tracked Changes and Compare Merge functions)
- Familiar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software
Benefits
Comp & perks- health coverage
- paid holidays
- variable bonus
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
technical writingmedical writingeditingregulatory complianceinformed consent formsdocument review
Soft Skills
collaborationmentoringorganizational compliance