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Research Data Coordinator
Job in
Washington, District of Columbia, 20022, USA
Listed on 2026-08-02
Listing for:
Jobtailor
Full Time
position Listed on 2026-08-02
Job specializations:
-
Science
Clinical Research
Job Description & How to Apply Below
- Responsible for data management for phase I, II, and III oncology clinical trials
- Support all aspects of clinical research data management for clinical trials
- Collect data from source documents and medical records
- Complete case report forms per sponsor requirements
- Review and analyze information from medical records to extract data
- Accurately capture data in electronic or paper Case Report Forms
- Ensure query resolution with proper physician and clinical study team oversight
- Request and upload radiological images into sponsor-provided imaging platforms
- Collect and organize source documents in electronic and paper format
- Ensure accuracy of data entered in the Clinical Trials Management System
- Interface with study team members to resolve discrepancies
- Schedule sponsor monitoring and study close‑out visits
- Provide support during internal and external monitoring and auditing preparation
- Communicate with pharmaceutical sponsors, study monitors, auditors, physicians, and study team members
- Collaborate closely with physicians and Study Coordinators to maintain protocol integrity
- Assist with training of incoming Research Data Coordinators
- High School Diploma or GED required
- Three (3) to five (5) years of related experience required
- Strong attention to detail
- Reliable and able to prioritize competing responsibilities
- Ability to work independently and function within a team
Demonstrates expertise in data management for oncology clinical trials, ensuring accuracy and compliance with sponsor requirements while effectively collaborating with study teams and external stakeholders.
Highest-signal resume keywords- Data Management
- Clinical Trials Management System
- Case Report Forms
- Attention to Detail
- Collaboration with Physicians
Hard Skills
- Data Collection
- Data Analysis
- Query Resolution
- Data Entry
- Source Document Organization
- Strong Attention to Detail
- Reliable
- Ability to Prioritize
- Independent Work
- Team Functionality
- Oncology Clinical Trials
- Clinical Research
- Monitoring and Auditing
- Protocol Integrity
- Imaging Platforms
- Electronic Case Report Forms
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