Job Description:
• Review clinical and laboratory data for accuracy, consistency, and completeness
• Identify discrepancies requiring clarification from study sites
• Apply clinical, laboratory, or patient-care knowledge to identify implausible or inconsistent data
• Write and issue data queries to sites using provided guidelines and templates
• Cross-check data across lab results, concomitant medications, adverse events, and medical history
• Review medical coding with guidance from senior reviewers
• Flag data quality trends, protocol compliance issues, and training needs
• Support audit readiness by following SOPs and maintaining accurate documentation
• Participate in Protocol Deviation, Data Review and Quality Team (DRQT), and Safety Monitoring Team (SMT) meetings
• Assist with listings, trackers, and slides for data review meetings
Requirements:
• Educated to Associate or Bachelor's level, or hold a diploma or certificate with relevant hands-on experience, in a life sciences, laboratory, or allied health field
• 0-2 years of experience in a clinical, laboratory, dental, or healthcare setting, including internships, clinical placements, or externships
• Comfortable reading and interpreting patient data such as vital signs, lab values, medication and allergy lists, treatment or procedure notes, or charts
• Familiar with medical terminology and accurate documentation practices
• Clear communicator in written and spoken English, with strong attention to detail
• Organized, able to track multiple tasks and meet deadlines
• Proficient in MS Excel and Office tools
• Relevant certification or licensure is nice to have
• Experience with EHR/EMR, practice management, or LIMS systems is nice to have
• Interest in oncology or other specialty areas is nice to have
Benefits:
• Training provided in clinical trial processes, clinical database navigation, query writing, and medical coding
• Mentorship as you build confidence
• Remote work arrangement