Oncology Trials: Clinical Research Data Associate

UT Health San Antonio; San Antonio (TX); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision care

Disability insurance

Flexible Spending Accounts

Retirement plan

Paid time off

Job summary

UT Health San Antonio is seeking a Clinical Research Assistant - Associate to accurately enter patient data from clinical trials into sponsor or local databases. You will locate required information in patient records, ensure data accuracy, and collaborate with the research team to resolve queries.

You will coordinate monitoring visits and participate in study teleconferences to maintain communication flow.

Qualifications

• Bachelor's degree is required.
• Ability to communicate and liaise with research participants, research team members, and other stakeholders.
• Strong organization and coordination skills within schedule constraints.
• Experience monitoring complex projects concurrently is a plus.
• Familiarity with medical terminology and clinical documentation practices.

Responsibilities

• Ensures accurate, complete, and compliant documentation of patient encounters and study data.
• Obtains required external records and laboratory results for research purposes.
• Addresses data discrepancies with clinicians and team members to maintain data integrity.
• Maintains confidentiality of patient information and supports source documents and templates.
• Adheres to data management plans and enters data into CRFs and databases; verifies source documentation.
• Troubleshoots data entry issues, responds to queries, and enters SAE data as required.

Skills

Communication

Organizational skills

Time management

Data entry

Team collaboration

Education

Bachelor's degree

Tools

MS Excel

Database systems

Microsoft Word

Outlook/Email

Job description

UT Health San Antonio is seeking a Clinical Research Assistant - Associate to accurately enter patient data from clinical trials into sponsor or local databases. You will locate required information in patient records, ensure data accuracy, and collaborate with the research team to resolve queries.

You will coordinate monitoring visits and participate in study teleconferences to maintain communication flow.