Data Capturer

**Data Capturer**

Assists with the accurate data capture and processing of paper and electronic source documentation that facilitates data review and analysis within a clinical trial setting. Your file preparation and other administrative duties in maintaining data management processes will be called upon.

**Technical Work Responsibilities**
- Complies with SA GCP and other clinical trial regulations
- Generate study files and required study documentation
- Record all paper forms received
- Reviews paper forms for completeness, accuracy and consistency
- Capturing the data accurately from paper and electronic source into a project specific database according to Aurum specific guidelines
- Verifies data from paper and electronic source with data already captured on the electronic database
- Supports the data management team in all data management functions
- Adheres to all data management SOP’s, guidelines and confidentiality agreements
- Completes daily time sheets
- Implements a filing system for study-related case report forms and other documentation

**Duties**
- Liaise with internal stakeholders regarding any challenges experienced
- Liaise with internal stakeholders regarding any possible solutions or recommendations to enhance productivity
- Cooperate with external stakeholders as and when required
- Generate study files and required study documentation
- Record all paper forms received
- Review paper forms for completeness, accuracy and consistency
- Capture data accurately from paper forms into a project specific database according to Aurum specific guidelines
- Verify data from paper forms with data already captured on the electronic database
- Track/log all paper forms received in-house in the in-house tracking/logging system
- Support the data management team in daily tasks
- Adhere to all data management SOP’s, guidelines and confidentiality agreements
- Complete daily time sheets
- Implement a filing system for study-related case report forms and other documentation
- Compile weekly and monthly statistic reports
- File study related case report forms and other documentation
- Participate in proactive team efforts to achieve departmental and company goals
- Identify any personal developmental requirements to enhance efficiency
- Implement approved solutions to enhance productivity
- Comply with all safety policies, practices and procedures
- Report all unsafe activities to Senior Management/Human Resources
- Adhere to decision making procedure

**Education**
- Grade 12

**Experience**
- One-year experience in data capturing

**Requirements**:

- Advanced computer skills
- Advanced Microsoft office skills

**Advantageous**
- SA GCP trained
- Clinical Trial experience
- Experience using various Clinical Research Databases (i.e. REDCap, Nukleus, DFnet, IMedidata, THREAD, etc.)