Clinical Research Assistant - 252386
Behavioral Health Market Context
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Job Description
missing data. Enter data into CRF/eCRF systems per sponsor guidelines and resolve queries in a timely manner. Collaborate with clinical staff and support sponsor monitoring visits and study meetings. Contribute to team training, process improvements, and other assigned tasks.
Qualifications:
Bachelor’s degree or equivalent experience with 2–3+ years in clinical research. Knowledge of GCP and QC processes, strong attention to detail, communication, and problem-solving skills. Proficient in Microsoft Office and able to work independently and within a team.
Additional Details:
• Location: Walnut Creek, CA (94598)
• Hours: Monday-Friday; Onsite 5 Days a week; Normal Business Hours
• Employment: Direct Hire
• Pay Range: $25/hr-$30/hr ($52,000-$62,000 Annual Salary) - Dependent on Background and Years of experience
Qualifications:
Bachelor’s degree or equivalent experience with 2–3+ years in clinical research. Knowledge of GCP and QC processes, strong attention to detail, communication, and problem-solving skills. Proficient in Microsoft Office and able to work independently and within a team.
Additional Details:
• Location: Walnut Creek, CA (94598)
• Hours: Monday-Friday; Onsite 5 Days a week; Normal Business Hours
• Employment: Direct Hire
• Pay Range: $25/hr-$30/hr ($52,000-$62,000 Annual Salary) - Dependent on Background and Years of experience
Qualifications
- •Bachelor’s degree or equivalent experience with 2–3+ years in clinical research
- •Knowledge of GCP and QC processes, strong attention to detail, communication, and problem-solving skills
- •Proficient in Microsoft Office and able to work independently and within a team
Benefits
- •Pay Range: $25/hr-$30/hr ($52,000-$62,000 Annual Salary) - Dependent on Background and Years of experience
Responsibilities
- •Support quality control and data entry for clinical research charts, ensuring accurate, complete, and timely data submission while maintaining site standards
- •Review study charts for accuracy and compliance with SOPs, GCP, and protocols; identify and escalate discrepancies or missing data
- •Enter data into CRF/eCRF systems per sponsor guidelines and resolve queries in a timely manner
- •Collaborate with clinical staff and support sponsor monitoring visits and study meetings
- •Contribute to team training, process improvements, and other assigned tasks
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