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Study Coordinator Jobs in Texas (NOW HIRING)

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Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Position Summary The Clinical Research Coordinator will support daily clinical trial operations ... Key Responsibilities * Conduct and document study visits per protocol, GCP, and site SOPs

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of analytical and clinical studies involving Luminex in vitro diagnostic devices, planning and execution of ...

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of analytical and clinical studies involving Luminex in vitro diagnostic devices, planning and execution of ...

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 ...

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Study Coordinator information

See Texas salary details

$20.5K

$51.1K

$75K

How much do study coordinator jobs pay per year?

As of Aug 29, 2026, the average yearly pay for study coordinator in Texas is $51,104.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $58,200.00 per year, depending on experience, location, and employer.

What is a study coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What are some common challenges study coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

How much does a study coordinator make?

The average salary for a study coordinator in California is approximately $60,000 to $75,000 per year, depending on experience, education, and the specific healthcare or research setting. Salaries can vary based on certifications, such as CRC or CCRP, and the complexity of the studies managed.

What qualifications do you need to be a research study coordinator?

A research study coordinator typically needs a bachelor's degree in a health-related field such as nursing, biology, or psychology. Relevant experience in clinical research, strong organizational skills, and knowledge of regulatory requirements like Good Clinical Practice (GCP) are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).

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

The most popular types of Study jobs in Texas are:

What cities in Texas are hiring for Study Coordinator jobs?

Cities in Texas with the most Study Coordinator job openings:

Infographic showing various Study Coordinator job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 78% Physical, 3% Hybrid, and 19% Remote job distribution, with an average salary of $51,104 per year, or $24.6 per hour.

Clinical Study Coordinator

Clinical Research Solution LLC

Houston, TX • On-site

$49K - $59K/yr

Full-time

Medical

Posted 16 days ago

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Job description

Position Summary

The Clinical Research Coordinator will support daily clinical trial operations, including patient visits, regulatory compliance, data entry, and sponsor communication. This role requires strong organizational skills, attention to detail, and the ability to work in a fast‐paced research environment.

Key Responsibilities

  • Conduct and document study visits per protocol, GCP, and site SOPs
  • Coordinate patient scheduling, screening, enrollment, and follow‐up
  • Collect, process, and ship biological samples (blood, urine, plasma)
  • Maintain accurate source documentation and eCRF data entry
  • Manage investigational product accountability
  • Communicate with sponsors/CROs regarding queries and monitoring visits
  • Assist with regulatory submissions, logs, and essential documents
  • Ensure protocol adherence and patient safety at all times
  • Support recruitment efforts and pre‐screening activities
  • Prepare for monitoring visits, audits, and inspections
  • Required Qualifications
  • 1+ year of clinical research experience OR strong clinical background

Company Description

Clinical Research Solution LLC conducts clinical trials at the doctor offices