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Clinical Study Coordinator Jobs in Rosharon, TX (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

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Clinical Research Coordinator (CRC) LINQ Research, LLC Location: Pearland, TX -0 Onsite Job Type ... We specialize in chronic disease studies and pride ourselves on being nimble, collaborative, and ...

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Clinical Study Coordinator information

See Rosharon, TX salary details

$25.1K

$60.4K

$103.8K

How much do clinical study coordinator jobs pay per year?

As of Aug 23, 2026, the average yearly pay for clinical study coordinator in Rosharon, TX is $60,434.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,900.00 and $70,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study teams and liaising with stakeholders. These abilities ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, safeguarding both data integrity and participant safety.

What are some common challenges clinical study coordinators face when managing multiple studies at once?

Clinical Study Coordinators often juggle several studies simultaneously, which requires strong organizational and time-management skills. Challenges include prioritizing tasks, ensuring regulatory compliance across different protocols, and keeping accurate documentation for each study. Effective communication with investigators, sponsors, and participants is essential to prevent misunderstandings and maintain study timelines. Utilizing project management tools and maintaining up-to-date records can help coordinators stay on track and reduce stress.

What is the difference between Clinical Study Coordinator vs Clinical Research Associate?

AspectClinical Study CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften a bachelor's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageHospitals, clinics, research sitesPharmaceutical companies, CROs, biotech firms

While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.

What job categories do people searching Clinical Study Coordinator jobs in Rosharon, TX look for?

The top searched job categories for Clinical Study Coordinator jobs in Rosharon, TX are:

What cities near Rosharon, TX are hiring for Clinical Study Coordinator jobs?

Cities near Rosharon, TX with the most Clinical Study Coordinator job openings:

Infographic showing various Clinical Study Coordinator job openings in Rosharon, TX as of August 2026, with employment types broken down into 3% As Needed, 68% Full Time, 20% Part Time, 2% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $60,434 per year, or $29.1 per hour.

Clinical Study Coordinator

Clinical Research Solution LLC

Houston, TX • On-site

$49K - $59K/yr

Full-time

Medical

Posted 9 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