Clinical Research Assistant - 252386
Behavioral Health Market Context
Apply Nowvia ACRP Career Center
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
More Jobs
- School-Based SLP | Apex, North Carolinaat BlazerJobs
- ID 6619 - Speech Language Pathologist - 1.0 FTE for 191 days/yearat Lake Oswego Public Schools
- Senior Quality Assurance Analystat Houston Methodist
- Remote Senior Project Lead, Oncology & Hematology Trialsat Syneos Health/ inVentiv Health Commercial LLC
- Clinical Research Front Desk Specialist - Patient Conciergeat CenExel
- Director of Clinical Research and Real World Evidenceat Virta Health
- Behavior Technician / Registered Behavioral Analyst Interventionist - Amazing Pay!at Footprints Behavioral Interventions
- Clinical Trials Coverage Analystat Virtual Vocations Inc
- Clinical Research Associateat CEDARS-SINAI
- Remote Clinical Research Programat Care Health