1

Clinical Data Coordinator Jobs in Spring, TX (NOW HIRING)

As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas ... in coordination with Quality and IT teams. Support validation activities including IQ/OQ/PQ ...

Be Seen First

Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Position Summary The Clinical Research Coordinator will support daily clinical trial operations, including patient visits, regulatory compliance, data entry, and sponsor communication. This role ...

next page

Showing results 1-20

Clinical Data Coordinator information

See Spring, TX salary details

$14

$26

$50

How much do clinical data coordinator jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical data coordinator in Spring, TX is $26.38, according to ZipRecruiter salary data. Most workers in this role earn between $20.34 and $30.14 per hour, depending on experience, location, and employer.

What does a clinical data coordinator do?

A Clinical Data Coordinator is responsible for collecting, managing, and ensuring the quality of data generated from clinical trials and medical research studies. They work closely with clinical research teams to input, verify, and monitor data accuracy, integrity, and compliance with regulatory standards. Their work is vital for the successful analysis of clinical trial outcomes and for supporting the development of new medical treatments.

What does a clinical data coordinator do?

A clinical data coordinator is responsible for overseeing a number of data related tasks associated with running a clinical facility. In this career, your job duties include creating reports on patient data, developing programs that support a clinical study, and providing information to ensure regulatory compliance on behalf of the clinic. The qualifications needed to have a career as a clinical data coordinator include a bachelor's degree in computer science or a related field. You also need strong analytical skills and experience working with databases.

How does a clinical data coordinator typically collaborate with other teams during a clinical trial?

Clinical Data Coordinators work closely with clinical research associates, data managers, and regulatory teams to ensure the accurate collection and management of trial data. They frequently communicate with site staff to resolve data discrepancies and ensure adherence to protocol and data quality standards. Regular meetings and updates are common to address ongoing data queries, share progress, and align on timelines. This cross-functional collaboration is vital for maintaining the integrity of clinical trial data and supporting successful study outcomes.

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

To thrive as a Clinical Data Coordinator, you need strong analytical skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory standards such as GCP and FDA guidelines are essential. Excellent organizational skills, effective communication, and the ability to collaborate with multidisciplinary teams help set top candidates apart. These competencies ensure accurate data collection and integrity, which are crucial for the success and compliance of clinical trials.

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

AspectClinical Data CoordinatorClinical Research Associate
Primary RoleManage and ensure accuracy of clinical data collection and entryOversee clinical trial sites, monitor study progress, and ensure compliance
Required CredentialsTypically a bachelor's degree in health, life sciences, or related fieldUsually a bachelor's degree in health sciences, along with monitoring certifications
Work EnvironmentData management teams, clinical trial databases, research organizationsClinical sites, monitoring visits, regulatory agencies
Industry UsageCommon in clinical data management and research organizationsCommon in pharmaceutical companies and contract research organizations

The Clinical Data Coordinator focuses on managing and verifying clinical data accuracy, while the Clinical Research Associate monitors trial sites and ensures compliance. Both roles are essential in clinical research but differ in daily responsibilities and focus areas.

What are the most commonly searched types of Clinical Data jobs in Spring, TX?

The most popular types of Clinical Data jobs in Spring, TX are:

What are popular job titles related to Clinical Data Coordinator jobs in Spring, TX?

For Clinical Data Coordinator jobs in Spring, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Data Coordinator jobs in Spring, TX look for?

The top searched job categories for Clinical Data Coordinator jobs in Spring, TX are:

What cities near Spring, TX are hiring for Clinical Data Coordinator jobs?

Cities near Spring, TX with the most Clinical Data Coordinator job openings:

Infographic showing various Clinical Data Coordinator job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $54,876 per year, or $26.4 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 12 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

14th 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


What MD Anderson Cancer Center employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom