Research Data Coordinator

Georgetown University Center on Education and the Workforce

Research Data Coordinator managing data for phase I, II, and III oncology clinical trials at Georgetown University. Collaborating with clinical research teams and ensuring compliance with research protocols.

Posted 7/21/2026full-timeWashington • District of Columbia, Washington • 🇺🇸 United StatesMid-LevelSenior💰 $18 - $27 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

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 ManagementClinical Trials Management SystemCase Report FormsAttention to DetailCollaboration with Physicians

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CollectionData AnalysisQuery ResolutionData EntrySource Document Organization

Soft Skills

Strong Attention to DetailReliableAbility to PrioritizeIndependent WorkTeam Functionality

Tools & Technologies

Imaging PlatformsElectronic Case Report Forms

Industry Keywords

Oncology Clinical TrialsClinical ResearchMonitoring and AuditingProtocol Integrity

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

Medical insurance
Dental insurance
Vision insurance
Disability insurance
Life insurance
Retirement savings
Tuition assistance
Work-life balance benefits
Employee discounts
Voluntary insurance options