Clinical Research Chart Reviewer

Benefits

Qualifications

• •The ideal candidate is comfortable independently reviewing medical records, interpreting clinical information (labs, medications, history), and applying study-specific inclusion and exclusion criteria
• •This role is well-suited for International Medical Graduates (IMGs), foreign-trained physicians (MD), or clinically experienced professionals seeking hands-on U.S. clinical research experience
• •Strong knowledge of medical terminology, clinical documentation, labs, and medications
• •Experience reviewing medical records, clinical data, or patient documentation
• •Ability to interpret and apply clinical research protocols
• •High attention to detail and ability to meet deadlines in a fast-paced environment
• •Strong critical thinking and decision-making skills
• •Familiarity with HIPAA, GCP, and human subjects research
• •Proficiency in Microsoft Office (Word, Excel, Outlook) and EMR systems
• •Opportunity to build relationships with investigators and research professional
• •Qualified candidates will be asked to complete a brief chart review or eligibility assessment exercise as part of the interview process
• •reviewing medical records: 3 years (Required)
• •reviewing clinical data & patient documentation: 3 years (Required)
• •Pearland, TX 77584 (Required)
• •11 more items(s)

Responsibilities

• •We are seeking a detail-oriented and clinically knowledgeable Medical Records Chart Reviewer to support patient eligibility and data accuracy across active clinical trials
• •Review patient medical records, including medical history, laboratory results, medications, and clinical notes
• •Apply study-specific inclusion and exclusion criteria to determine patient eligibility
• •Make independent eligibility assessments with oversight from the research team
• •Verify accuracy and completeness of clinical data in alignment with study protocols
• •Maintain consistent <24-hour turnaround times for assigned chart reviews
• •Identify and resolve discrepancies in collaboration with clinical and research staff
• •Ensure strict compliance with HIPAA, GCP, and FDA regulatory requirements
• •Maintain organized and thorough documentation of all reviews
• •Chart review accuracy (QA audited)
• •Turnaround time compliance
• •Protocol adherence
• •Documentation quality and completeness
• •Full-time, Monday–Friday (8:00 AM – 5:00 PM)
• •11 more items(s)