Clinical Research Data Entry Specialist
The Clinical Research Data Entry Specialist plays a vital role in the success of clinical trials by accurately capturing, managing, and maintaining data.
* Responsibilities:
* Enter trial data into electronic capture systems with precision and attention to detail.
* Review source documents and case report forms for completeness and accuracy.
* Perform data validation and query resolution in collaboration with study coordinators and investigators.
* Maintain confidentiality and security of patient and study information.
* Support data cleaning activities and contribute to database lock processes.
* Communicate effectively with research staff to clarify data discrepancies.
Required Skills and Qualifications:
* High school diploma or equivalent required; associate or bachelor's degree in health sciences, life sciences, or related field preferred.
* Minimum of 1–2 years of experience in clinical research or data entry, preferably in a healthcare or academic setting.
* Familiarity with clinical trial documentation and EDC systems (e.g., REDCap, Medidata, OpenClinica).
* Strong organizational skills and attention to detail.
* Ability to work independently and manage multiple tasks under tight deadlines.
* Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
* Understanding of medical terminology and clinical research processes is a plus.
Benefits:
* Attractive salary + benefits.
Duration: 3-month contract. Location: East Melbourne.