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Clinical Research Associate Jobs in Rosharon, TX

Shriners Children's

Clinical Research Coordinator

Galveston, TX · On-site

$22.75 - $30.25/hr

The Clinical Research Coordinator, Level 1 (CRC I) is a research professional responsible for supporting the oversight and compliance of both system-wide and local Shriners Children's (SHC) clinical ...

FOCUSPOINT

Clinical Research Coordinator

Webster, TX · On-site

Clinical Research Coordinator Location: Multiple Locations - TX, VA, FL Employment Type: Contract - 6 months Pay: Up to $35 per hour About FOCUSPOINT: FOCUSPOINT specializes in connecting top-tier ...

Alcanza

Clinical Research Coordinator

Sugar Land, TX

$21.75 - $29/hr

A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and ...

Alcanza

Clinical Research Coordinator

Sugar Land, TX

$21.75 - $29/hr

A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and ...

Icon plc

CRA II and Senior CRA

Houston, TX · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and ...

panoramic

Clinical Research Coordinator II

Pasadena, TX · On-site

$20.75 - $27.50/hr

Clinical Research Coordinator II Renal Specialists of Houston Pasadena, Texas Advance Your Clinical Research Career in a Growing Nephrology Research Program Renal Specialists of Houston is seeking an ...

Panoramic Health

Clinical Research Coordinator II

Pasadena, TX · On-site

$20.75 - $27.50/hr

Clinical Research Coordinator II Renal Specialists of Houston Pasadena, Texas Advance Your Clinical Research Career in a Growing Nephrology Research Program Renal Specialists of Houston is seeking an ...

aQua Dialysis

Clinical Research Coordinator

Houston, TX · On-site

$23.25 - $30.75/hr

Responsible for education of clinic staff regarding clinical research. · May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. · Communicates with ...

BioTalent

Clinical Research Coordinator II

Bellaire, TX · On-site

$21.75 - $29/hr

Clinical Research Coordinator II Location: Bellaire, TX Schedule: Full-Time | Onsite 5 Days per Week Position Overview We are seeking an experienced Clinical Research Coordinator II (CRC II) to ...

New

BioTalent

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator II Location: Houston, TX Schedule: Full-Time | Onsite 5 Days per Week Position Overview We are seeking an experienced Clinical Research Coordinator II (CRC II) to ...

New

aQua Dialysis

Clinical Research Coordinator

Houston, TX · On-site

$23.25 - $30.75/hr

Responsible for education of clinic staff regarding clinical research. • May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. • Communicates with ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Rosharon, TX

Clinical Research Associate information

See Rosharon, TX salary details

$10

$36

$62

How much do clinical research associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical research associate in Rosharon, TX is $36.80, according to ZipRecruiter salary data. Most workers in this role earn between $25.82 and $47.12 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Rosharon, TX as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 3% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $76,540 per year, or $36.8 per hour.

Clinical Research Coordinator

Shriners Children's

Galveston, TX • On-site

$22.75 - $30.25/hr

Full-time

Re-posted 7 days ago

Shriners Children's rating

8.0

Company rating: 8.0 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

137th of 1,061 rated hospitals

Job description

Company Overview
Shriners Children's is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.
With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family's ability to pay or insurance status. Please click here to learn more about our locations.
Job Description
The Clinical Research Coordinator, Level 1 (CRC I) is a research professional responsible for supporting the oversight and compliance of both system-wide and local Shriners Children's (SHC) clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and collaborating with the Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice (GCP) guidelines, when applicable.
The CRC works collaboratively with investigators, research staff, and clinical teams to ethically recruit and consent Shriners Children's vulnerable pediatric research participants and to appropriately collect, manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and the quality and integrity of study data.
Key Responsibilities:
  • Supports the implementation and conduct of approved research protocols, ensuring studies are performed in compliance with the protocol, Good Clinical Practice (GCP), applicable regulatory requirements, and SHC policies and standards.
  • Performs study-specific research activities and/or interventions within the bounds of professional licensure and training.
  • Assists with participant recruitment, screening, informed consent/assent, scheduling, and coordination of study visits.
  • Coordinates the collection and documentation of research data.
  • Maintains regulatory documentation and study records in accordance with institutional policies and sponsor requirements.
  • Supports communication and coordination between investigators, sponsors, monitors, and institutional departments involved in research activities.
  • Assists investigators with the development and submission of investigator-initiated research protocols and related regulatory documentation.
  • Contributes to study progress reports, monitoring visits, audits, and preparation of study results or presentations when applicable.
  • Ensures appropriate training and education are completed in order to safely perform study-related procedures and protocol requirements.

Required Qualifications:
  • 1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)

Preferred Qualifications:
  • Bachelor's degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field
  • Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)
  • Experience coordinating intergroup or multi-site clinical studies
  • CCRP or CCRC certification
Compensation is determined based on years of relevant experience and departmental equity.

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