Impact-Driven Clinical Trials: Quality & Data Analyst

Green Life Science; Covina (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

Green Life Science is seeking a QC & Data Analyst in Covina, CA to ensure data accuracy and study compliance. The role focuses on data review, reconciliation, and timely query resolution within CRF/eCRF systems.

You will collaborate with CRCs, investigators, sponsors and CRO teams to uphold data integrity. The candidate should have 1–3+ years in clinical or biological research, a Bachelor’s degree or equivalent, and proven skills in Excel, Word and Outlook.

Qualifications

• 1–3+ years’ experience in clinical or biological research
• Bachelor’s degree or equivalent experience
• Understanding of GCP and clinical research processes
• Experience with clinical data, source documentation, CRFs/eCRFs or QC
• Strong Excel, Word and Outlook skills
• Excellent attention to detail and organisation
• Strong communication and problem-solving skills
• Comfortable working independently in a fast-paced clinical research environment

Responsibilities

• Review study charts against SOPs, GCP, GDP and study protocols
• Identify missing, inconsistent or discrepant data
• Enter and verify data within CRF/eCRF systems
• Perform source-to-CRF/eCRF reconciliation
• Raise and resolve data queries
• Support sponsor monitor visits and query resolution
• Attend Site Initiation Visits (SIVs)
• Identify data trends and support QC reporting
• Work closely with CRCs, investigators, sponsors and CRO teams
• Support onboarding, training and process improvement

Skills

Experience in clinical or biological研究

Attention to detail

Communication

Problem solving

Independent work in fast-paced env

Education

Bachelor’s degree or equivalent experience

Tools

Excel

Word

Outlook

Job description

Green Life Science is seeking a QC & Data Analyst in Covina, CA to ensure data accuracy and study compliance. The role focuses on data review, reconciliation, and timely query resolution within CRF/eCRF systems.

You will collaborate with CRCs, investigators, sponsors and CRO teams to uphold data integrity. The candidate should have 1–3+ years in clinical or biological research, a Bachelor’s degree or equivalent, and proven skills in Excel, Word and Outlook.