We are seeking a detail-oriented and analytical Clinical Research Analyst to support clinical studies and trials through data analysis, documentation, and reporting. The ideal candidate will be responsible for collecting, organizing, and interpreting clinical data to support research objectives and regulatory compliance.
Collect, clean, and analyze clinical trial data from various sources
Ensure accuracy and integrity of data entered into clinical databases
Assist in designing study protocols, case report forms (CRFs), and data collection tools
Prepare statistical summaries, charts, and reports for internal teams and regulatory submissions
Collaborate with clinical research coordinators, investigators, and regulatory teams
Monitor ongoing studies to ensure protocol compliance and data quality
Support the development of research publications, abstracts, and presentations
Conduct literature reviews and stay updated on clinical and scientific advancements
Maintain documentation in accordance with Good Clinical Practice (GCP) and ICH guidelines
Assist in audit preparation and regulatory inspections as needed
Bachelors degree in Life Sciences, Public Health, Biostatistics, or a related field
2+ years of experience in clinical research, clinical data analysis, or related role
Familiarity with GCP, ICH guidelines, and clinical trial processes
Proficiency in Microsoft Excel and statistical software (e.g., SAS, SPSS, R)
Strong analytical, problem-solving, and organizational skills
Excellent written and verbal communication skills
High attention to detail and ability to work independently or in a team
Masters degree in Clinical Research, Biostatistics, or Epidemiology
Experience with EDC systems (e.g., Medidata, REDCap, Oracle Clinical)
Certification in clinical research (e.g., CCRP, ACRP)
Knowledge of regulatory requirements (FDA, EMA, etc.)
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