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Clinical Research Associate Jobs in Spring, TX (NOW HIRING)

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Clinical Research Coordinator II

Houston, TX

$23.25 - $30.75/hr

How This Role Makes a Difference The Clinical Research Coordinator 's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely ...

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Clinical Research Associate information

See Spring, TX salary details

$10

$36

$62

How much do clinical research associate jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for clinical research associate in Spring, TX is $36.60, according to ZipRecruiter salary data. Most workers in this role earn between $25.67 and $46.83 per hour, depending on experience, location, and employer.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education, such as a degree in life sciences or healthcare, and experience with clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or training programs.

What are Clinical Research Associates?

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, and why are they important?

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 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.

What is the work of Clinical Research Associate?

A Clinical Research Associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate with investigators, review trial data, conduct site visits, and ensure compliance, often using electronic data capture systems. CRAs play a key role in maintaining trial quality and integrity throughout the study process.

How much does a CRC make?

A Clinical Research Associate (CRA) in Houston typically earns between $60,000 and $85,000 annually, depending on experience, certifications, and the complexity of the clinical trials. Entry-level CRAs may start around $55,000, while experienced professionals with specialized skills can earn over $90,000. Salaries often include benefits such as health insurance and travel allowances, and the role requires knowledge of Good Clinical Practice (GCP) and clinical trial management tools.

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.

Can you be a CRA with no experience?

Becoming a Clinical Research Associate (CRA) typically requires some background in healthcare, life sciences, or related fields, but entry-level positions may be available for candidates with strong organizational skills and relevant certifications such as GCP training. Most employers prefer candidates with some related experience or education, but internships or training programs can provide a pathway for those without prior CRA experience.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Spring, TX? The most popular types of Clinical Research jobs in Spring, TX are:
What are popular job titles related to Clinical Research Associate jobs in Spring, TX? For Clinical Research Associate jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Spring, TX look for? The top searched job categories for Clinical Research Associate jobs in Spring, TX are:
What cities near Spring, TX are hiring for Clinical Research Associate jobs? Cities near Spring, TX with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you

Clinical Research Infusion Nurse

INTEGRITY ADVANCED THERAPEUTICS PLL

Houston, TX

$25 - $42/hr

Per diem

Posted 16 days ago

Job description

Job Title: Clinical Research Infusion Nurse

Location: Houston, TX
Department: Clinical Research @ Integrity Advanced Therapeutics PLLC
Reports To: Principal Investigator / Clinical Research Manager
Job Type: Contract – Per Diem
License Required: Active RN License in the State of Texas
Certification Required: Good Clinical Practice (GCP) Certification

Position Summary:

The Clinical Research Infusion Nurse plays a critical role in the execution of clinical trials by safely administering investigational medications or placebos to study participants. This position ensures the integrity of the research process while prioritizing patient safety and comfort. The nurse collaborates closely with investigators, clinical research coordinators, and other healthcare professionals to deliver high-quality care in compliance with clinical protocols and regulatory standards.

Key Responsibilities:

Administering Infusions

  • Prepare patients for infusion procedures.
  • Administer investigational drugs or placebos via infusion pumps.
  • Monitor patients during and after infusions for adverse reactions.

Monitoring Patients

  • Assess and document vital signs and clinical status.
  • Identify and report any changes in patient condition to the Principal Investigator and Clinical Research Coordinator.

Maintaining Safety

  • Ensure a safe and comfortable environment for patients.
  • Respond promptly to medical emergencies and adverse events.
  • Adhere strictly to clinical trial protocols and safety guidelines.

Communication

  • Maintain clear and compassionate communication with patients.
  • Collaborate effectively with investigators, coordinators, and study staff.

Ensuring Protocol Adherence

  • Administer treatments in strict accordance with study protocols.
  • Maintain accurate and timely documentation of all procedures and observations.

Education

  • Educate patients about their treatment plans, potential side effects, and trial participation.

Medication Management

  • Prepare and dilute investigational medications as per protocol.
  • Maintain inventory and ensure proper storage and handling of infusion supplies.

Skills and Qualifications:

  • Registered Nurse (RN) licensed in the State of Texas (Required)
  • GCP Certification (Required)
  • Infusion Therapy Expertise: Proficient in IV insertion and infusion pump operation.
  • Clinical Trial Knowledge: Familiarity with clinical research protocols, regulatory compliance, and ethical standards.
  • Strong Clinical Judgment: Skilled in-patient assessment and emergency response.
  • Excellent Communication: Able to convey complex information clearly to patients and team members.
  • Detail-Oriented: Accurate in medication preparation, documentation, and protocol adherence.
  • Independent and Team-Oriented: Capable of working autonomously while contributing to a collaborative research environment.
  • Compassionate Care: Provides emotional support and reassurance to patients undergoing treatment.

Preferred Qualifications:

  • Prior experience in a clinical research setting.
  • Prior GI/Liver Nursing experience
  • Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).