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Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

This is a full time position. The CRA will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical ...

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How much do full time h1b clinical research jobs pay per year?

As of Aug 31, 2026, the average yearly pay for full time h1b clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a full time H1B clinical research position?

A Full Time H1B Clinical Research position refers to a clinical research job in the United States that is filled by an employee who is sponsored under the H1B visa program. This allows qualified foreign professionals, typically with a background in science or medicine, to work legally in the U.S. on clinical research projects. The position is considered full time, meaning the employee works the standard number of weekly hours set by the employer, and the job entails conducting, managing, or supporting clinical trials and research studies. Employers must meet certain requirements to sponsor an H1B visa, including demonstrating that the job requires specialized knowledge.

What are some common challenges faced by H1B clinical research professionals working full-time in the U.S.?

Full-time H1B Clinical Research professionals often navigate challenges such as adapting to new regulatory environments, managing complex documentation for both clinical trials and visa compliance, and balancing the demands of rigorous study protocols with tight timelines. Additionally, collaboration with multidisciplinary teams requires strong communication skills, especially when working with colleagues from diverse backgrounds. Many also find the need to stay up-to-date with evolving FDA and IRB requirements, which can be demanding but is essential for career advancement.

What are the key skills and qualifications needed to thrive as a full time H1B clinical research professional, and why are they important?

To thrive as a Full Time H1B Clinical Research professional, you typically need a degree in life sciences or a related field, experience with clinical trials, and eligibility to work under H1B sponsorship. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are often required. Strong organizational skills, attention to detail, and the ability to communicate effectively with cross-functional teams set candidates apart. These skills and qualifications are crucial for ensuring regulatory compliance, data integrity, and the successful execution of clinical studies.
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Full Time H1B Clinical Research jobs near you
Infographic showing various Full Time H1B Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Cypress, TX • On-site

Horizon Clinical Research
See more jobs at Horizon Clinical Researchexternal

$37K - $47K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

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Job description

We are seeking an experienced and detail oriented Clinical Research Assistant (CRA) for our Cypress, TX and Houston, TX office. This is a full time position. The CRA will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical research timeline from pre-site visit (PSV) through study close-out. Duties include, but are not limited to:

  • Recruits patients for clinical research studies based on study inclusion/exclusion.
  • Obtains informed consent from subject and conducts the screening visit.
  • Completes paperwork related to subject visits.
  • Pack & ship samples to laboratories.
  • Enrollment and follow up of eligible subjects according to protocol requirements.* Coordinate and conduct subject visits.
  • Assure all procedures are conducted in compliance with the clinical protocol and standard operating procedures (SOPs)
  • Work closely with Principal Investigators (PIs) to assure subjects receive appropriate medical evaluation and care.
  • Attend sponsor investigator meetings as needed for assigned clinical trials.* Perform blood draws and taking patient vital signs.
  • Completion of study documents, including electronic data entry.
  • Communicate professionally and timely with all relevant staff involved in the clinical research study.
  • Other duties as assigned.
  • Qualifications:
  • Bachelors degree preferred. Foreign Qualified Doctors encouraged to apply
  • Phlebotomy and ECG experience( Preferred)
  • Previous experience as a Clinical Research Coordinator.
  • Excellent verbal and written communication skills, including medical terminology.
  • Professional, self starter and well organized.
  • Attention to detail.
  • Strong computer skills.

Job Type: Full-time

Benefits:


  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance


Application Question(s):


  • Are you a foreign medical graduate?


Education:


  • Bachelor's (Preferred)


Experience:


  • Clinical research: 1 year (Preferred)


Work Location: In person