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Job Description
Research Data Coordinator II (RDC II) |
The Tone:
This is a fully proficient role focused on clinical trial data management. This position is crucial for ensuring data integrity and compliance for industry, cooperative, and investigator-initiated clinical trials by accurately extracting and synthesizing information from various medical records. The role involves performing all core Research Data Coordinator functions and offers significant opportunity for career growth.
The TL;DR
• Role: Full Time
• Type: Full-time
• Mission: Ensure data integrity and compliance for clinical trials through meticulous data extraction, synthesis, and management.
What You’ll Actually Do
• Data Extraction: Review and synthesize diverse medical records, including clinic notes and pathology reports, to accurately extract trial data as specified by research protocols.
• Protocol Adherence: Manage protocol-specific data requirements for multiple research projects, ensuring all data capture aligns with regulatory standards and Good Clinical Practice (GCP).
• Complex Task Management: Routinely handle complex tasks related to data management, such as determining methods for data requirements, resolving queries, and ensuring accurate data capture.
• Collaboration: Collaborate effectively with study coordinators and monitors to ensure a clear understanding and strict adherence to protocol requirements.
• Mentorship & Workload: Oversee a higher patient volume and/or trials of greater complexity, while also contributing to the development of less experienced team members through support and mentorship.
• Presentations: Present relevant information in department meetings as appropriate.
The Must-Haves
• Background: High School Diploma/GED or an AA/AS degree with a foundational understanding of clinical or research data management principles.
• Experience: Three (3) years of data management experience required, OR one (1) year of clinical or research data management experience with an AA/AS degree.
• Skills: Data extraction and synthesis, adherence to research protocols, Good Clinical Practice (GCP), Federal regulations compliance, query resolution, and data integrity.