Day-to-Day Responsibilities
Design the clinical trial database and data entry screens (electronic data capture or EDC) according to the study protocol
Write and maintain the data management plan and related standard operating procedures
Review incoming trial data, check it against validation rules and identify missing or inconsistent entries
Raise data queries with trial sites, follow them up and record how each one was resolved
Coordinate with clinical monitors, biostatisticians, medical coders and safety teams on data issues
Code adverse events and medical terms using standard dictionaries such as MedDRA, under the guidance of senior staff
Prepare the database for locking, complete final reconciliation and maintain an audit trail for regulatory inspections


