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Clinical Research Data Manager Jobs in Spring, TX

DM Clinical Research

Research Assistant

Houston, TX

$18.25 - $25.25/hr

Research Assistant The Research Assistant will be responsible for assisting the clinical research ... Assisting in the collection and recording of patient data per Sponsor requirements via the ...

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Spring, TX

Clinical Research Data Manager information

See Spring, TX salary details

$43.6K

$95.5K

$168.2K

How much do clinical research data manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for clinical research data manager 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 are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

What is the difference between Clinical Research Data Manager vs Clinical Research Coordinator?

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a clinical research data manager, and why are they important?

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.
What are the most commonly searched types of Clinical Research Data jobs in Spring, TX? The most popular types of Clinical Research Data jobs in Spring, TX are:
What are popular job titles related to Clinical Research Data Manager jobs in Spring, TX? For Clinical Research Data Manager jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Research Data Manager jobs in Spring, TX look for? The top searched job categories for Clinical Research Data Manager jobs in Spring, TX are:
What cities near Spring, TX are hiring for Clinical Research Data Manager jobs? Cities near Spring, TX with the most Clinical Research Data Manager job openings:
Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 14% Part Time, and 1% Contract. Highlights an 93% Physical, 3% 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 14 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).