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

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Contract Clinical Research information

See Spring, TX salary details

$43.6K

$95.5K

$168.2K

How much do contract clinical research jobs pay per year?

As of Aug 9, 2026, the average yearly pay for contract clinical research in Spring, TX is $95,517.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $109,000.00 per year, depending on experience, location, and employer.

What is a contract clinical research?

A Contract Clinical Research job involves working on a temporary or project-based basis to support clinical trials and research studies. Professionals in this role ensure compliance with regulatory standards, oversee study protocols, and manage data collection and reporting. They often work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. These roles require expertise in clinical trial processes, good clinical practices (GCP), and regulatory guidelines. Contract positions vary in duration and may offer flexibility in location and work arrangements.

What are the key skills and qualifications needed to thrive in the contract clinical research position, and why are they important?

To thrive in Contract Clinical Research, you need a strong background in clinical trial processes, regulatory compliance (such as GCP/ICH guidelines), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like CCRA or CCRC are often required. Excellent organizational, communication, and problem-solving skills are vital for managing multiple projects and collaborating with cross-functional teams. These abilities ensure the smooth and ethical conduct of clinical trials while meeting tight timelines and quality standards.

What are the typical day-to-day responsibilities for someone in a contract clinical research role?

In a Contract Clinical Research position, you will typically oversee the execution of clinical trials, which includes tasks such as monitoring study sites, ensuring regulatory and protocol compliance, and managing study documentation. You'll collaborate closely with principal investigators, sponsors, and clinical site staff to ensure timelines are met and data is collected accurately. Responsibilities may also include preparing reports, assisting with site selection or initiation, and resolving any study-related issues that arise. This dynamic role often requires balancing administrative, technical, and interpersonal tasks to successfully support clinical research projects.

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 Contract Clinical Research jobs in Spring, TX? For Contract Clinical Research jobs in Spring, TX, the most frequently searched job titles are:
What cities near Spring, TX are hiring for Contract Clinical Research jobs? Cities near Spring, TX with the most Contract Clinical Research job openings:
Infographic showing various Contract Clinical Research job openings in Spring, TX as of July 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $95,517 per year, or $45.9 per hour.

Clinical Research Infusion Nurse

INTEGRITY ADVANCED THERAPEUTICS PLL

Houston, TX

$25 - $42/hr

Per diem

Re-posted 12 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).