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Electronic Data Capture Jobs in Texas (NOW HIRING)

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Research Coordinator, Rheumatology

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 ...

Stryde Research

Entry Level Research Nurse

Plano, TX · On-site

... electronic data capture (EDC) systems Perform Venipuncture, blood collection, IV line placement and infusion Screen, enroll, and obtain informed consent from eligible study participants Administer ...

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 ...

Stryde Research

Entry Level Research Nurse

Plano, TX · On-site

Perform patient assessments, collect vital signs, and document findings accurately in electronic data capture (EDC) systems * Perform Venipuncture, blood collection, IV line placement and infusion

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 ...

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 ...

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How much do electronic data capture jobs pay per hour?

As of Aug 21, 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 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 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 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?

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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 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,031 per year, or $25 per hour.

Clinical Data Monitor I - Hybrid

Caris Life Sciences

Irving, TX • On-site

Full-time

Posted 8 days ago

Job description

At Caris, we understand that cancer is an ugly word-a word no one wants to hear, but one that connects us all. That's why we're not just transforming cancer care-we're changing lives.
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: "What would I do if this patient were my mom?" That question drives everything we do.
But our mission doesn't stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare-driven by innovation, compassion, and purpose.
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Job Description
Position Summary
The Clinical Data Monitor is responsible for clinical data management activities for the Caris sponsored and collaborating protocols and projects. This role ensures the highest standards of data integrity and quality in support of critical research efforts to improve treatment, health, and medical outcomes for oncology patients. The Clinical Data Monitor I provides support to both external and internal research coordinators in patient enrollment, data collection, and data query resolution. Responsibilities include oversight and management of clinical investigative sites in accordance with Federal Code of Regulations, Good Clinical Practices (GCP), Good Registry Practices (GRP), ICH Guidelines, local regulations, and applicable Compliance and Sponsor SOPs.
Job Responsibilities
  • Maintains proficient knowledge of Electronic Data Capture (EDC) systems to support training, change proposals, and user acceptance testing.
  • Establish and maintain strong working relationships with site data and regulatory coordinators.
  • Perform quality control review of submitted Case Report Forms (CRFs), including source document verification and issuance of data queries.
  • Serve as an evaluator for internal Clinical Research Coordinators in training and provide detailed, constructive feedback.
  • Maintain regulatory documentation for all assigned sites and study staff.
  • Create and manage site records within the EDC for newly onboarded sites.
  • Conduct quality control audits of the clinical database.
  • Ensure compliance with GCP guidelines, FDA, Institutional Review Board (IRB), HIPAA regulations, site operating procedures, and ethical standards for the conduct of clinical research.
  • Collaborate closely with onsite teams to confirm appropriate consenting is completed and documented prior to data abstraction.
  • Communicate effectively with research teams, investigators, study sponsors, and ancillary staff.

Required Qualifications
  • Requires 3-5 years of experience in data collection activities within a GCP regulated clinical research environment.
  • Proficient in Microsoft Office Suite
  • Experience working with Electronic Data Capture (EDC) systems.
  • Clinical study experience in oncology.
  • Strong understanding of medical terminology.
  • Ability to work independently and make sound decisions.
  • Strong organizational skills with the ability to prioritize, meet deadlines, and manage multiple projects simultaneously.
  • Demonstrated ability to build trust with site personnel and communicate effectively with diverse stakeholders.
  • High attention to detail with a passion for contributing to meaningful research outcomes for patients.
  • Strong problem solving skills and the ability to deliver practical solutions.
  • Excellent written and verbal communication skills in English.
  • Professional demeanor with positive, collaborative interactions with internal and external partners.
  • Ability to propose, implement, and evaluate appropriate resolutions to issues.

Preferred Qualifications
  • Bachelor's degree preferred
  • Research Coordinator certification (SoCRA, ACRP)
  • Working knowledge of human anatomy.

Physical Demands
  • Ability to sit and or stand for extended periods of time.
  • Ability to lift routine office supplies and operate standard office equipment.

Training
All job specific, safety, and compliance training will be assigned based on the responsibilities associated with this position, including but not limited to:
  • Good Clinical Practices (GCP)
  • Human Subject Protection (HSP) Training
  • SEER Primary Site Training
  • Multiple Primary and Histology Rules
  • AJCC Staging

Other
  • At times, may be required to work weekends/holidays.

Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management's assignment of essential functions. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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