Job Description

Data Management:

• Collect and manage clinical trial data from different sources, like forms and electronic systems.
• Make sure the data is accurate, complete, and entered on time.
• Check for errors or mismatches in the data and work with the research team to fix them.
• Help get the data ready for analysis.

Study Documentation:

• Keep study files organized and up-to-date, following all rules and regulations.
• Make sure all required documents, like consent forms and approvals, are current and ready for audits.
• Track important dates and deadlines for the study.

Compliance & Quality Control:

• Review data to make sure it follows study rules and Good Clinical Practice (GCP) guidelines.
• Help prepare for visits and audits from regulatory agencies.
• Ensure the study meets all legal, ethical, and privacy standards.

Collaboration & Communication:

• Work with investigators, coordinators, and other team members to support the study.
• Communicate with outside groups like sponsors, CROs, and regulators to keep data flowing smoothly.
• Create regular updates on how the study is going, including any issues with the data.

Job Tags

Similar Jobs