Research Data Specialist - Investigational Cancer Therapeutics

MD Anderson Cancer Center • Houston, TX

418d • Onsite

About The Position

The Research Data Specialist position at The University of Texas MD Anderson Cancer Center is designed to support large-scale, multi-protocol, multi-institutional clinical trial projects. The role involves collaborating with research teams and the Principal Investigator to ensure protocol compliance, data integrity, and effective communication of relevant information. The specialist will also provide training and orientation to new and existing research staff, contributing to the overall success of clinical research initiatives.

Requirements

• Bachelor's degree in a related field is required.
• Two years of research study experience is required, or equivalent experience may substitute for education.
• A Master's degree in a related field is preferred, with no experience required.

Nice To Haves

• Experience with electronic data capture systems.
• Familiarity with clinical trial protocols and regulations.
• Strong analytical and problem-solving skills.

Responsibilities

• Perform accurate and timely data entry and analysis for clinical trials.
• Serve as a subject matter expert for the departmental Research Data team.
• Transfer patient information into electronic databases and maintain data accuracy.
• Review medical records to extract necessary data points for research.
• Develop and maintain protocol-specific tools and study materials.
• Ensure consistency between protocol databases and source documentation.
• Conduct source document verification and drug accountability.
• Coordinate meetings with Principal Investigators and research teams to review study status.
• Generate research reports to support oversight by the Investigator.
• Coordinate routine monitoring visits with internal and industry representatives.
• Lead during audits and provide timely responses to queries.
• Conduct internal clinical trial monitoring according to policies and procedures.
• Participate in quality assurance initiatives for clinical research.
• Onboard, mentor, and train new research data staff.
• Communicate with the Principal Investigator regarding deadlines and meetings.
• Identify training gaps and develop educational presentations.
• Assist in all aspects of the clinical trial process from startup to closeout.
• Support financial reconciliation and regulatory compliance efforts.
• Assist in writing protocols, grants, and manuscript submissions.

Benefits

• Relocation assistance available.
• Hybrid work environment.
• Competitive salary range from $48,000 to $72,000.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Ambulatory Health Care Services
• Education Level: Bachelor's degree