Clinical Research Specialist, GCP & FDA Regulated Trials
Overview
Own the execution of clinical trials from initiation to completion, ensuring data integrity, patient safety, and regulatory compliance at SJHMC. You will coordinate study activities, recruit participants, collect data, and document CRFs while aligning with GCP and FDA guidelines. This on-site role is centered in Phoenix, AZ, within a collaborative research ecosystem including Barrow Neurological Institute and Norton Thoracic Institute. What sets this role apart is the emphasis on humankindness and a mission-driven culture that supports professional growth and global health impact.
What You'll Do5
- 1Build and manage trial activities, including participant recruitment and data collection, to drive high-quality study outcomes
- 2Coordinate subject visits and ensure adequate supplies and investigator availability to maintain study timelines
- 3Educate study subjects and families with study-specific information to support informed consent and engagement
- 4Collect and process protocol required specimens and complete CRFs accurately and on time
- 5Serve as liaison between Sponsor, Investigator, and Study Subject to ensure seamless communication across stakeholders
Requirements5
- 1Associates Degree in related field or equivalent experience
- 2Minimum two years related clinical research experience
- 3Regulatory knowledge including GCP and FDA guidelines
- 4Strong organizational skills and attention to detail
- 5Ability to work on-site in Phoenix, AZ
Salary Insight
$50 - $75k per year
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