Remote Clinical Research Source Writer – QA/Regulatory

Arizona Liver Health; Chandler (AZ); Hybrid; USD 50,000 - 70,000; Full time

Benefits offered by this job

Health, Dental, Vision with HSA plans

401K with 6% company match

Educational Assistance

Short & Long Term Disability

Shared company vehicles

Job summary

A leading health research institute is seeking an experienced Source Writer with QA/QC/Regulatory expertise. You will ensure high standards of scientific excellence while contributing to transformative liver health initiatives. Responsibilities include generating source documents, performing QA reviews, and ensuring compliance with clinical research regulations. The ideal candidate will have a relevant degree and experience in clinical research. Competitive salary and benefits offered including health insurance, 401K match, and educational assistance.

Qualifications

• Proven knowledge of SOPs and GCPs.
• Basic knowledge of medical terminology.
• Experience in clinical research quality assurance and compliance.

Responsibilities

• Extract information from clinical research protocols.
• Ensure source documents are complete and accurate.
• Perform QA reviews of subject charts.

Skills

Critical thinking

Independence

Understanding clinical research protocols

Experience in building clinical research documents

Education

Associate or Bachelor's degree in healthcare or related field

Job description

A leading health research institute is seeking an experienced Source Writer with QA/QC/Regulatory expertise. You will ensure high standards of scientific excellence while contributing to transformative liver health initiatives. Responsibilities include generating source documents, performing QA reviews, and ensuring compliance with clinical research regulations. The ideal candidate will have a relevant degree and experience in clinical research. Competitive salary and benefits offered including health insurance, 401K match, and educational assistance.