Overview
We're an early-stage startup building out our operations, and we're looking for an experienced Quality Assurance professional to review our documentation on an occasional, as-needed basis. This is a flexible, project-based engagement ideal for someone with spare capacity who wants light, intermittent work rather than a full-time role.
The core focus is straightforward: review our standard operating procedures (SOPs) and work instructions, and provide clear, actionable feedback.
Responsibilities
- Review existing SOPs and work instructions for clarity, completeness, and alignment with quality standards
- Identify gaps, inconsistencies, or areas needing improvement
- Provide written feedback and practical recommendations
- Advise on quality best practices as they relate to clinical data management
Requirements
- Minimum 3 years of experience in a quality role, ideally within clinical research or a related regulated environment
- Familiarity with Clinical Data Management processes (hands-on data management experience not required)
- Working knowledge of clinical trial documentation and quality standards
- Strong attention to detail and clear written communication
- Able to work independently with minimal oversight
Engagement Terms
This is an ad hoc contract position. There is no guarantee of full-term employment or a set number of hours. Work will be assigned as needed, making this well suited to someone looking for flexible, occasional work alongside other commitments.
Compensation: $30–$40 per hour, commensurate with experience.
Pay: $25.00 - $40.00 per hour
Work Location: Remote
