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Electronic Data Capture Jobs in Texas (NOW HIRING)

GI Alliance

Research Associate (31682)

Austin, TX · On-site

$17 - $18/hr

... electronic data capture - EDC) in accordance with applicable regulations and sponsor requirements • Perform study-specific readings and measurements including but not limited to: o Vital signs o ...

Driscoll

HEDIS Coordinator

Corpus Christi, TX · On-site

... use of electronic clinical data as it relates to DHP Quality performance metrics. This position ... capture. ESSENTIAL DUTIES AND RESPONSIBILITIES: The HEDIS Coordinator develops and implements ...

Neuralink

Preclinical Study Coordinator

Austin, TX

Familiarity with electronic data capture systems or GLP-compliant documentation platforms. Additional Requirements and Competencies: * Willingness to work in an animal research facility environment ...

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How much do electronic data capture jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for electronic data capture in Texas is $25.01, according to ZipRecruiter salary data. Most workers in this role earn between $13.95 and $31.50 per hour, depending on experience, location, and employer.

What is an electronic data capture?

An Electronic Data Capture (EDC) job involves managing digital systems used to collect, store, and process clinical trial or research data. Professionals in this role ensure data accuracy, integrity, and compliance with regulatory standards. They may configure EDC systems, troubleshoot technical issues, and support researchers or study personnel in data entry and validation. Strong analytical, technical, and problem-solving skills are essential in this position.

What are the key skills and qualifications needed to thrive in an electronic data capture position?

To thrive in Electronic Data Capture, you need a solid understanding of clinical data management, data entry accuracy, and regulatory compliance, often supported by a degree in life sciences or information technology. Familiarity with EDC systems such as Medidata Rave or Oracle InForm, as well as certifications like Certified Clinical Data Manager (CCDM), are commonly required. Attention to detail, strong organizational skills, and effective communication are valuable soft skills in this field. These competencies are important for ensuring the integrity, security, and efficiency of electronic clinical trial data collection and management.

What are the typical daily responsibilities of an electronic data capture professional?

Professionals in Electronic Data Capture are responsible for designing and managing electronic case report forms (eCRFs), monitoring data entry for accuracy and completeness, and ensuring compliance with clinical trial protocols and regulatory standards. Daily tasks may also include troubleshooting EDC system issues, coordinating with clinical research teams, and preparing data reports for study progress reviews. Collaboration with data managers, IT specialists, and regulatory staff is common, so teamwork and clear communication are essential. Staying organized and detail-oriented helps ensure the integrity and quality of collected data, which is critical for the success of clinical research projects.

What are the most commonly searched types of Electronic Data Capture jobs in Texas? The most popular types of Electronic Data Capture jobs in Texas are:
What are popular job titles related to Electronic Data Capture jobs in Texas? For Electronic Data Capture jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Electronic Data Capture jobs in Texas look for? The top searched job categories for Electronic Data Capture jobs in Texas are:
Electronic Data Capture jobs near you
Infographic showing various Electronic Data Capture job openings in Texas as of August 2026, with employment types broken down into 85% Full Time, 7% Part Time, and 8% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,031 per year, or $25 per hour.

Research Associate (31682)

GI Alliance

Austin, TX • On-site

$17 - $18/hr

Part-time

Posted 25 days ago

GI Alliance rating

6.4

Company rating: 6.4 out of 10

Based on 69 frontline employees who took The Breakroom Quiz

640th of 887 rated healthcare providers

Job description

Review and follow Urology AllianceStandard Operating Procedures
• Read and understand specific requirements of each study protocol and informed consent form
• Works with study coordinators and other research team members to complete protocol specific procedures and documentation
• Assists in clinic and protocol administration duties including but not limited to:
o Conduct screening procedures and other visit procedures in a timely and accurate manner
o Provide instructions to patients to ensure proper protocol compliance
o Distribute and instill study medications in compliance with protocol randomization requirements
o Learn and understand lab procedures and obtain and process study related lab specimens according to the study specific manuals (lab and procedural)
o Use approved source documents; obtain protocol-specific data to complete and maintain source documents and case report forms (including electronic data capture - EDC) in accordance with applicable regulations and sponsor requirements
• Perform study-specific readings and measurements including but not limited to:
o Vital signs
o ECG
o Urine Pregnancy Test
o Uroflow, PVR, urinalysis, cystoscopy
o Photography and videography
o Catheter placement
• Reports irregular readings and measurements to Investigator and Lead Study Coordinator
• Package and ship laboratory specimens to study-specific destinations
• Complete applicable training requirements and ongoing education as required
• Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc.
• Communicate with and support patients and their families as necessary.
• Must have or gain knowledge of relevant software/programs
• Assist with the development of source documents and phone screen tools
• Manage ancillary supply inventory and assist with drug accountability as needed
• Maintain HIPAA compliant communication and confidentiality, at all times
• Performs other duties as assigned
Must be willing to gain a thorough knowledge and follow strict adherence of all clinical study protocols.
• Develop an understanding of and demonstrate Good Clinical Practices (GCPs), learn and comply with all FDA clinical trial and IRB rules and regulations
• Effective time management and the ability to prioritize work
• Excellent communication skills and the ability to interact with all levels of management, staff, and physicians in person, virtually, and in writing
• Ability to be flexible with the day-to-day job requirements to facilitate a successful workflow in clinic

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