Clinical Quality Assurance Professional
2 days ago
- Provide QA expertise during study calls, including protocol deviation meetings, risk-based quality management discussions, and study operations and trial oversight meetings.
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation within Veeva QMS.
- Manage and track quality processes, address QA-related questions from study teams in real time, and provide clear guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
Job Description
We are seeking a highly experienced Quality Assurance Specialist to join our team. The ideal candidate will have a strong foundation in Good Clinical Practice (GCP) and the ability to guide study teams in maintaining compliance.
Required Skills and Qualifications
- Education: Bachelor's degree in life sciences or related discipline; an advanced degree is preferred.
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong background in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS.
Benefits
This full-time contract role offers 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
Contract Opportunity
The contractor must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
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