Data Management Associate
11 hours ago
We are seeking a skilled Data Management Associate to join our team at Staff Unlimited Recruitment.
Role Overview
The successful candidate will be responsible for maintaining and enhancing the performance and quality of data management services, including database set-up, CRF tracking, review, validation, and updating data in clinical databases for paper and EDC studies. They will also assist in the development of data management-relevant study documents.
Key Responsibilities
- CRF Tracking and Scanning: Set-up and testing of tracking databases, ensuring accuracy and efficiency.
- Data Entry Support: Providing assistance with data entry, verifying discrepancies, and creating data entry guidelines.
- Database Set-up Activities: Supporting the creation of CRFs, setting up and testing study databases, developing test cases for data entry screens, and conducting plausibility checks.
- Validation of CRF, Query, and External Data: Ensuring the accuracy and integrity of data.
- Creation and Management of Queries: Identifying and resolving issues related to CRF or external data.
- External Data Reconciliation: Verifying the consistency of external data.
- Quality Control Tasks: Participating in quality control activities for CRF data.
- Team and Project Meetings: Contributing to team discussions and project progress meetings.
- Clinical Data Manager Support: Collaborating with Clinical Data Managers on data-related tasks.
- Process Improvements: Identifying opportunities for process enhancements and implementing changes.
Optional/Developmental Job Functions
- SAE Reconciliation: Resolving discrepancies between source and electronic data capture systems.
- User Account Management: Managing user accounts and permissions.
- User Training and Documentation: Creating training materials and documentation for EDC studies.
- eClinical Project Manager Support: Assisting the eClinical Project Manager with data-related tasks.
Requirements
- Education or Experience: Holding a degree or possessing relevant experience in medical documentation or a related field.
- GCP Knowledge: Understanding Good Clinical Practice requirements and regulatory guidelines in drug research.
- Computer Skills: Proficiency in data management software, MS Word, Excel, and the Internet.
- Problem-Solving and Teamwork: Demonstrating problem-solving skills and ability to work independently and collaboratively as part of a team.
Salary Range: $65,000 - $85,000 per annum, depending on experience. We offer a competitive salary and benefits package that aligns with industry standards.
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