Clinical Research Data Entry Specialist
4 weeks ago
Renstar Medical Research, a leading clinical research site, is seeking a full-time Clinical Trial Medical Data Entry Specialist / Quality Control Specialist. The ideal candidate will have a strong understanding of medical terminology, medical conditions, and medications, as well as excellent communication and organizational skills.
- Perform Quality Assurance and Control to maintain audit readiness of studies
- Ensure all study-related communication is documented and identify any areas that need further clarification or inconsistencies to the Site Director
- Coordinate with site staff, vendors, and contract employees to obtain quality data
- Review Source Documents, CRF's, Study Documents, Logs, and Master Files with coordinators and staff to ensure quality, completeness, and accuracy
Key Responsibilities
- Review consent documents on assigned trials and source documents
- Compile review sheets for each CRF reviewed, which includes the error, a description of the correction (if necessary), and the name of the coordinator who is to make the correction
- Complete simple reports and reporting quality trends to management
- Work closely with monitors to facilitate timely turnaround of study queries and data entry
Requirements
- Excellent communication skills (interpersonal, written, verbal)
- Must be able to identify and communicate about research problems and processes across various levels of the organization
- Good organizational and interpersonal skills
- Attention to detail
- Must be self-motivated and able to perform tasks independently
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