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Electronic Data Capture Jobs in Texas (NOW HIRING)

Src

Research Coordinator

Dallas, TX

Collect, enter, and maintain accurate research data using REDCap, electronic data capture systems, electronic medical records (Epic preferred), and study databases to ensure data quality and ...

Easy Recruiter

Data Entry Specialist (Remote)

Houston, TX · On-site

$16.25 - $21.75/hr

Electronic data capture completion (EDC). * Quality control of EDC Source Data Verification * Gather data from multiple source documents and enter into electronic database system. * Address data ...

M/A/R/C Research, LLC

Regulatory Data Manager

Plano, TX · Remote

... electronic data capture (EDC) systems and online survey platforms. Ensure accurate mapping of protocol requirements into study databases and collection instruments. Manage study metadata, coding ...

M/A/R/C Research, LLC

Regulatory Data Manager

Plano, TX · On-site +1

... electronic data capture (EDC) systems and online survey platforms. • Ensure accurate mapping of protocol requirements into study databases and collection instruments. • Manage study metadata ...

ECN Operating LLC

Registered Nurse

Houston, TX

Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems. * Collaborate with study coordinators, investigators, and other research staff to ensure ...

New

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

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 ...

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How much do electronic data capture jobs pay per hour?

As of Aug 9, 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 Coordinator

Scottish Rite for Children

Dallas, TX • On-site

Full-time

Posted 23 days ago

Scottish Rite For Children rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

299th of 1,055 rated hospitals

Job description

Our patients are our number one priority! We're committed to giving children back their childhood!
Job Posting Title:
Research Coordinator
Location:
Dallas - Hospital
Additional Posting Details:
Monday - Friday,
8:00am - 4:00pm
Job Description:
Duties/Responsibilities
  • Collaborate with staff in other research divisions and clinical departments within Scottish Rite to obtain the information and support necessary to conduct research. Organize and lead project meetings, communicate study updates, and provide regular reports to Principal Investigators.
  • Perform literature reviews, assist with study design, prepare regulatory documents, consent forms, and research submissions for presentations and publications.
  • Prepare, submit, and maintain regulatory documentation with the Institutional Review Board (IRB), Research Advisory Panel, and other applicable regulatory agencies, including initial submissions, continuing reviews, amendments, and study closures, while ensuring compliance with Good Clinical Practice (GCP), Human Subjects Protection, and applicable regulatory guidelines.
  • Develop and maintain project timelines, communicate barriers proactively, and coordinate with research teams to ensure milestones and deadlines are achieved.
  • Execute approved study protocols in accordance with GCP, institutional policies, and study requirements. Maintain regulatory binders, source documentation, and study files; manage reportable events, protocol deviations, adverse events, and audit readiness for internal, sponsor, and regulatory inspections.
  • Screen, recruit, consent, and enroll research participants while ensuring compliance with study protocols and regulatory requirements.
  • Coordinate study visits and procedures, including clinic visits, questionnaires, laboratory collections, imaging, and other protocol-required assessments. Monitor participant follow-up and protocol compliance.
  • Collect, enter, and maintain accurate research data using REDCap, electronic data capture systems, electronic medical records (Epic preferred), and study databases to ensure data quality and integrity. Resolve data queries and maintain study documentation.
  • Generate reports and organize data for statistical analysis.
  • Assist with the preparation and submission of abstracts, posters, presentations, manuscripts, and grant or funding applications.
  • Participate in internal, sponsor, and regulatory audits; identify process improvement opportunities and support corrective actions as appropriate.
  • Participate in onboarding, training, and coordinating research staff, interns, students, residents, and fellows.
  • Read literature relevant to pediatric medical and surgical conditions and attend conferences and educational meetings supporting ongoing research initiatives.
  • Support research activities across divisions, departments, or campuses as needed.
  • Perform other duties as assigned.

Required Skills/Abilities
  • Bachelor's degree required.
  • Prior clinical research and regulatory experience strongly preferred; three years of clinical research experience preferred.
  • Certification as a Certified Clinical Research Professional (CCRP) preferred.
  • Working knowledge of Good Clinical Practice (GCP), Human Subjects Protection, IRB processes, and clinical research regulatory requirements preferred.
  • Experience with REDCap or other electronic data capture systems preferred.
  • Experience with electronic medical records, particularly Epic, preferred.
  • Proficiency in Microsoft Office.
  • Strong organizational, time management, and project coordination skills with the ability to manage multiple studies simultaneously.
  • Excellent communication, problem-solving, critical thinking, and attention to detail.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.
  • Self-motivated, adaptable, resourceful, and able to thrive in a fast-paced research environment.
  • Capable of recruiting research participants in person, by phone, and virtually.

Preferred Qualifications for Advanced/Senior Research Coordinators
  • Candidates with experience in IND/IDE studies, audit readiness, quality management, CAPA development, multi-site study coordination, SOP development, staff mentoring, project management, and sponsor interactions are encouraged to apply.

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