Clinical Research

• Ensures the implementation of clinical trials in compliance with standards
• Acts as primary site contact and manager throughout clinical research phases
• Develops strong site relationships
• Performs site management and monitoring activities
• Participates in site selection and qualification activities
• Conducts site visits and prepares reports in a timely manner
• Communicates with investigators and site staff
• Manages documentation in CTMS, eTMF, and other systems

Associate Specialist, Clinical Research

• Responsible for the planning, performance, report and documentation of statistical tasks during the study process.
• Assist in the development of Study Protocols, CRFs and reports/manuscripts by providing statistical input.
• Write and review the statistical sections in the Study Protocol.
• Ensure CRF design meets specific statistical requirements.
• Perform sample size calculations and define randomisation procedures.
• Write the Statistical Analysis Plan and design the Data Presentation Plan.
• Plan and execute statistical analysis according to protocols.

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Associate Specialist, Clinical Research

Biostatistician