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Clinical Research Data Manager Jobs in Spring, TX

Clinical Research Coordinator

Houston, TX · On-site

$23.25 - $30.75/hr

Overview The Clinical Research Coordinator drives clinical research strategy and execution across ... Manage Regulatory Compliance and Data Integrity. Direct preparation and submission of regulatory ...

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

Resolve data management queries and correct source data within sponsor provided timelines * Assist ... Minimum Experience: * 3 years prior Clinical Research Coordinator experience required * Prefer 1 ...

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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 Sep 7, 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 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 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 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 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 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:

Infographic showing various Clinical Research Data Manager job openings in Spring, TX as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $95,517 per year, or $45.9 per hour.

Coordinator, Research Data - Lymphoma Myeloma

MD Anderson

Houston, TX • On-site

$21.15 - $26.44/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago


MD Anderson Cancer Center rating

8.5

Company rating: 8.5 out of 10

Based on 172 frontline employees who took The Breakroom Quiz

12th of 898 rated healthcare providers


Job description

Research Data Coordinator The Research Data Coordinator supports the Lymphoma Observational & Translational Research (LOTR) program within the Department of Lymphoma and Myeloma at The University of Texas MD Anderson Cancer Center. This role focuses on delivering high-quality patient-facing research support and precise clinical data abstraction for lymphoma and myeloma standard-of-care research initiatives. The Research Data Coordinator works closely with patients, clinicians, and research teams to ensure data integrity, protocol compliance, and accurate documentation.

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. As part of UT MD Anderson, the Research Data Coordinator contributes directly to advancing translational and observational research efforts that improve outcomes for patients with lymphoma and myeloma. The Research Data Coordinator is expected to work independently with limited oversight while maintaining strong collaboration with multidisciplinary clinical and research teams.

The Research Data Coordinator plays a critical role in patient engagement, clinical research operations, and biospecimen coordination. This Research Data Coordinator position is fully onsite and embedded within a fast-paced clinical research environment dedicated to excellence in cancer research and patient care. The ideal candidate is detail-oriented and passionate about data quality, with an interest in clinical research and patient interaction; education, work experience, and licenses or certifications align with the minimum requirements for a research data coordinator role, with the ability to learn disease-specific concepts, follow human subject research guidelines, and perform responsibilities with professionalism and accountability.

Minimum $21.15 - Midpoint $26.44 - Maximum $31.73 per hour Work Location: Onsite, Houston, TX Typical work schedule: Days Why Us. This role offers the opportunity to contribute meaningfully to patient-centered research that advances scientific understanding and improves care for individuals with lymphoma and myeloma. UT MD Anderson supports professional growth through hands-on research experience, interdisciplinary collaboration, and a mission-driven environment that values excellence, learning, and balance

Employer-paid medical coverage starting day one for employees working 30+ hours/week, plus optional group dental, vision, life, AD&D, and disability insurance. Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options. Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.

Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Clinical Research Support Perform informed consent procedures for minimal risk research protocols in accordance with institutional policies and research guidelines Educate patients on research studies and assist them in considering enrollment when eligibility criteria are met Assist patients in completing study questionnaires and required study procedures Screen and identify patients based on protocol eligibility and exclusion criteria Data Entry and Clinical Data Abstraction Develop detailed knowledge of lymphoma disease processes, treatments, biomarkers, and clinical prognostics Interpret and accurately abstract disease-specific and outcomes data from clinician notes, imaging, laboratory values, pathology reports, and other EMR documentation Record outcomes of study visits and complete required documentation in study databases per protocol and institutional guidelines Translational Research Support Screen for and identify standard-of-care biospecimen collections required for research Coordinate, collect, process, and distribute research biospecimens in a timely manner Enter research-related order requests in the EMR and ensure availability of supplies for clinical staff Collaborate with clinical trial teams to support successful biospecimen collection and processing Professional Competencies Apply analytical thinking to gather information, break down problems, and support sound decision-making Demonstrate professionalism through collaborative relationships with physicians and healthcare team members Promote teamwork by encouraging collaboration, valuing contributions, and balancing individual and team goals EDUCATION Required: High School Diploma or Equivalent Preferred: Bachelor's Degree WORK EXPERIENCE Required: 2 years Related experience or No experience required with preferred degree. The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.

This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment. It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law.http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html Additional Information Requisition ID: 180707 Employment Status: Full-Time Employee Status: Regular Work Week: Days Minimum Salary: US Dollar (USD) 44,000 Midpoint Salary: US Dollar (USD) 55,000 Maximum Salary : US Dollar (USD) 66,000 FLSA: non-exempt and eligible for overtime pay Fund Type: Soft Work Location: Onsite Pivotal Position: No Referral Bonus Available?: No Relocation Assistance Available?: No #LI-Onsite Apply


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