Responsibilities:

Responsible for clinical data processing as directed by Site Director or another assigned manager.
Quality control the clinical data to ensure the data quality and report discrepancies to the coordinator.
Complete any training as required by sponsor for access and approval to complete data entry.
Enter data as appropriate for protocol into paper or electronic case report forms.
Track to ensure that data entry is complete for subjects including completed study visits and related forms.

Skills and Qualifications:

Education and experience
- High School Diploma or equivalent
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- Knowledgeable in medical terminology so as to communicate with physician office and staff.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
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.
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

Data Entry Clerk

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