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Responsibilities:
- Coordinate regulatory compliance for clinical studies.
- Review clinical research protocols and prepare documents.
- Manage submissions for UCLA, FDA, and sponsor requirements.
- Work with monitors to process regulatory documents timely.
Requirements:
- 1+ years of experience as a clinical researcher.
- Strong interpersonal and communication skills.
- Ability to prioritize tasks and meet deadlines.
- Analytical skills to assess protocols and regulatory needs.
- Attention to detail in a fast-paced environment.
- Proficiency with Adobe and Microsoft suite software.
Benefits:
- Salary range of $60k-$120k USD.
- Fully remote work option.
- Career staff position with indefinite duration.
