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Essential Job Duties:
In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems. Responsibilities may include but are not limited to:
- Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software
- Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements
- Reporting any irregularities or problems with a study to the appropriate parties
- Supporting other clinical research-related activities
- Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines
- Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.