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Key Responsibilities:
- Pre-review and edit informed consent forms for FDA, HHS, and Health Canada compliance.
- Collaborate with IRB members and stakeholders to finalize document requirements.
- Perform quality-control reviews and mentor new editors on regulatory standards.
Requirements:
- Bachelor's degree and 2+ years of technical/medical editing experience.
- At least 1 year of IRB experience; CIP certification or willingness to obtain.
- Proficiency in Microsoft Word, Excel, and remote collaboration tools.
Benefits:
- Fully remote position within the United States.
- Base salary $66,767–$116,089 plus variable bonus potential.
- Health coverage and paid holidays included.
Partner Company
The partner company provides specialized services for clinical research and regulatory compliance. It fosters a collaborative environment and emphasizes ethical research practices, though team size is not specified.