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Edc Jobs in Austin, TX (NOW HIRING)

Info Way Solutions

Informatica Developer

Austin, TX · On-site

$52.75 - $69.50/hr

Required : • 10+ years of experience with Informatica tools including PowerCenter, IICS, IDMC, MDM, Axon, EDC, IDQ, Customer360, Supplier360, and Entity360. • 10+ years of experience establishing ...

Hirekeyz Inc

Systems Analyst

Austin, TX · On-site

... EDC and Axon, including glossaries, dashboards, data quality and discovery features, and advanced scanners 4 Required Knowledge of source-to-target data lineage mapping and automated harvest methods ...

GI Alliance

Research Associate (31682)

Austin, TX · On-site

$17 - $18/hr

... 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 ...

PSI CRO

Site Management Associate II

Austin, TX · On-site

Reviews site-specific EDC completion progress and provides the Monitor with regular updates * Serves as the main contact point for other company departments in administrative site-related issues

PSI CRO

Site Management Associate II

Austin, TX

Reviews site-specific EDC completion progress and provides the Monitor with regular updates * Serves as the main contact point for other company departments in administrative site-related issues

PSI CRO

Site Management Associate II

Austin, TX · On-site

Reviews site-specific EDC completion progress and provides the Monitor with regular updates * Serves as the main contact point for other company departments in administrative site-related issues

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Showing results 21-40

All JobsEdc JobsEdc Jobs in Austin, TX

Edc information

See Austin, TX salary details

$15

$26

$36

How much do edc jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for edc in Austin, TX is $26.06, according to ZipRecruiter salary data. Most workers in this role earn between $21.20 and $29.90 per hour, depending on experience, location, and employer.

What is an EDC?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.

What are the key skills and qualifications needed to thrive as an EDC specialist?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What are some common challenges faced by EDC professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are popular job titles related to Edc jobs in Austin, TX?

For Edc jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Edc jobs in Austin, TX look for?

The top searched job categories for Edc jobs in Austin, TX are:

What cities near Austin, TX are hiring for Edc jobs?

Cities near Austin, TX with the most Edc job openings:

Edc jobs near you
Infographic showing various Edc job openings in Austin, TX as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, and 5% Contract. Highlights an 77% Physical, 3% Hybrid, and 20% Remote job distribution, with an average salary of $51,821 per year, or $24.9 per hour.

Senior Clinical Research Coordinator

Tekton Research Inc

Austin, TX

$24 - $32/hr

Full-time

Posted 22 days ago

Key responsibilities

  • Manage multiple clinical trials from study start-up through close-out, ensuring protocol compliance and data integrity.

  • Serve as a primary contact for investigators, sponsors, monitors, vendors, and study teams, and coordinate study activities.

  • Recruit, screen, consent, enroll, and retain study participants while conducting study visits and specimen processing.

Job description

Senior Clinical Research Coordinator - Austin, Texas

Full-Time/Non-Exempt/On-Site

Position Summary

The Senior Clinical Research Coordinator (Senior CRC) is an experienced clinical research professional responsible for managing multiple clinical trials from study start-up through close-out. This role ensures protocol compliance, participant safety, data integrity, regulatory compliance, and successful study execution.

The Senior CRC serves as a key liaison between investigators, sponsors, monitors, participants, and research staff while providing guidance and mentorship to junior coordinators. The ideal candidate is highly organized, proactive, detail-oriented, and able to effectively manage multiple priorities.

Key Responsibilities
  • Independently coordinate and manage multiple clinical trials from start-up through close-out.
  • Serve as a primary site contact for investigators, sponsors, monitors, vendors, and study teams.
  • Recruit, screen, consent, enroll, and retain study participants according to protocol requirements.
  • Conduct study visits and perform pediatric and adult phlebotomy and specimen processing as required.
  • Monitor participant safety and appropriately document and report adverse events and protocol deviations.
  • Maintain accurate source documentation, regulatory files, and essential study records in compliance with GCP, FDA regulations, and ICH guidelines.
  • Prepare and submit IRB and regulatory documents, including amendments and continuing reviews.
  • Maintain accurate study data in EDC and CTMS systems and resolve data queries within required timelines.
  • Prepare for and support monitoring visits, sponsor audits, and regulatory inspections.
  • Identify and resolve study issues proactively to maintain timelines, quality, and compliance.
  • Mentor and provide guidance to Clinical Research Coordinators and other research staff.
  • Contribute to process improvement and overall site quality and performance.
Required Qualifications
  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, Clinical Research, or related field preferred.
  • 3-5+ years of clinical research experience, with demonstrated ability to independently coordinate clinical trials.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical research processes.
  • Experience managing multiple clinical trials and competing priorities.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with EDC systems, CTMS, and Microsoft Office.
  • Strong organizational, problem-solving, and communication skills.
  • Ability to work independently, exercise sound judgment, and collaborate effectively with multidisciplinary teams.
  • Commitment to participant safety, data integrity, and research quality.
Preferred Qualifications
  • Current ACRP or CCRC, or equivalent certification.
  • Bachelor's or advanced degree in a healthcare, public health, or clinical research field.
  • Experience with industry-sponsored and/or multi-center clinical trials.
  • Experience mentoring junior research staff.
  • Experience supporting sponsor audits, regulatory inspections, or complex monitoring activities.
  • Experience with participant recruitment and retention strategies.
Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We value professional development, collaboration, accountability, and meaningful contributions.

If you're an experienced clinical research professional ready to take on greater responsibility and help lead high-quality clinical trial execution, we encourage you to apply and become part of the Tekton Research team.


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