Clinical Research Data Coordinator — Oncology Trials

Socket.dev; San Antonio (TX); On-site; USD 52,000 - 76,000; Full time

Job summary

UT Health San Antonio is seeking a Clinical Research Assistant – Associate to enter patient data from clinical trials into sponsor and local databases, ensuring accuracy and integrity. You will locate required information in records, query data with the team, and coordinate monitoring visits with study monitors.

The role requires strong attention to detail, knowledge of clinical documentation, and ability to communicate with research participants and stakeholders.

Qualifications

• Bachelor's Degree in a basic science.
• Ability to communicate and liaise with research participants, team members, and stakeholders.
• Demonstrated ability to organize and coordinate work within schedule constraints.
• Familiarity with medical terminology and clinical documentation practices.
• Understanding of basic biostatistics and clinical data interpretation.
• Strong attention to detail and data accuracy.

Responsibilities

• Enter patient data promptly into sponsor or local databases.
• Locate information in patient records and ensure data accuracy.
• Collaborate with research team to resolve data queries.
• Coordinate monitoring visits with study monitors.
• Participate in teleconferences with sponsors and CROs.
• Maintain confidentiality and source documents/templates.
• Enter SAE data and respond to data management queries.

Skills

Communication

Organizational skills

Attention to detail

Time management

Data accuracy

Education

Bachelor's Degree in a basic science

Tools

Microsoft Word

Microsoft Excel

Outlook

Database systems

Job description

UT Health San Antonio is seeking a Clinical Research Assistant – Associate to enter patient data from clinical trials into sponsor and local databases, ensuring accuracy and integrity. You will locate required information in records, query data with the team, and coordinate monitoring visits with study monitors.

The role requires strong attention to detail, knowledge of clinical documentation, and ability to communicate with research participants and stakeholders.