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Research Helper Jobs in Texas (NOW HIRING)

UX Lead - Research & Insights

Fort Worth, TX · On-site

$100K - $125K/yr

This individual will collaborate with cross-functional teams to guide strategic decisions through qualitative and quantitative research, helping the organization deliver impactful business and ...

We're looking for a collaborative, detail-oriented Research Librarian to join our Research Services team to help deliver an exceptional employee experience. In this role, the Research Librarian is a ...

We're looking for a collaborative, detail-oriented Research Librarian to join our Research Services team to help deliver an exceptional employee experience. In this role, the Research Librarian is a ...

The Research team at TrustRadius is responsible for ensuring that we cover the right products, ask the right questions of reviewers, and turn important user insights and ratings into helpful sector ...

The Research team at TrustRadius is responsible for ensuring that we cover the right products, ask the right questions of reviewers, and turn important user insights and ratings into helpful sector ...

Research Psychologist Belong. Connect. Grow. with KBR! Around here, we define the future. We are a ... In this role, you will be a key scientist for helping NASA achieve its goals for human spaceflight ...

Research Psychologist Belong. Connect. Grow. with KBR! Around here, we define the future. We are a ... In this role, you will be a key scientist for helping NASA achieve its goals for human spaceflight ...

Showing results 21-40

Research Helper information

What are the most commonly searched types of Research jobs in Texas?

The most popular types of Research jobs in Texas are:

Infographic showing various Research Helper job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, 2% Contract, and 1% Nights. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution.

Senior Clinical Research Coordinator

Austin, TX

Tekton Research Inc
Scientific Research and Development Services • 11 - 50 employees

$24 - $32/hr

Full-time

Posted 28 days ago


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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