Clinical Data Analyst

Role & Responsibility:

Responsible for reviewing data based on the Clinical Data Analysis (CDA) plan for one or more studies

Additional responsibilities will include:

• Create a study specific CDA plan
• Review study data accurately to identify site performance issues,
• Communicate effectively with the project team, CRAs, DM Staff, Medical staff, Scientific Council to ensure adequate monitoring intervention and effective resolution of site performance issues.
• Work with Data Management, Clinical Operations, Central Laboratory, ITG, Biostatistics, Medical Writing, Regulatory Affairs and Quality Assurance to ensure all data collected within a clinical study are managed according to corporate standards and meet regulatory guidelines for data integrity.

Experience & Qualifications:

• The ideal candidate will have at least 3-4 years clinical data management or clinical research associate (CRA) experience. 
• Bachelor’s degree or local equivalent in a scientific discipline and/or appropriate experience
• Knowledge of regulatory requirements respecting data quality and clinical trials conduct.
• Must possess excellent oral communication skills and attentiveness to detail.
• Proven leadership skills and the ability to work independently to resolve study related issues
• Ability to work within a team environment and manage competing priorities in a changeable environment
• Knowledge of database technologies and processes.
• Ability to handle stressful situations and deadlines.
• Excellent interpersonal skills required