Clinical QA Specialist – Regulatory Documents

Integrated Resources Inc.; Collegeville (PA); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading staffing firm seeks a Clinical Data Quality Reviewer to ensure accuracy in clinical and regulatory documents. Candidates should have at least 3 years of relevant experience in clinical settings, focusing on data quality review and medical writing. Strong analytical, communication, and detail-oriented skills are essential for this role, offering an engaging environment within the healthcare industry.

Qualifications

• Minimum 3 years in clinical and data management experience in healthcare.
• Requires experience in medical writing and DQR/QC of clinical documents.
• Understanding of scientific principles and familiarity with medical terminology.

Responsibilities

• Perform DQR/QC on clinical study reports and regulatory documents.
• Document findings and prepare written reports of analysis.
• Participate in resolution of findings with the document authors.

Skills

Data Quality Review

Clinical Documentation

Medical Writing

Attention to Detail

Analytical Skills

Communication Skills

Education

BS degree or equivalent

Job description

A leading staffing firm seeks a Clinical Data Quality Reviewer to ensure accuracy in clinical and regulatory documents. Candidates should have at least 3 years of relevant experience in clinical settings, focusing on data quality review and medical writing. Strong analytical, communication, and detail-oriented skills are essential for this role, offering an engaging environment within the healthcare industry.