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Clinical Research Data Manager Jobs in Rosharon, TX

Clinical Research Coordinator II

Pasadena, TX · On-site

$20.75 - $27.50/hr

Manage assigned clinical trials in accordance with protocol requirements, Good Clinical Practice ... Collect, document, and enter study data accurately and in a timely manner. * Maintain source ...

Clinical Research Coordinator II

Bellaire, TX · On-site

$21.75 - $29/hr

Coordinate and manage assigned clinical trials from study start-up through completion. * Develop a ... Help ensure participant safety and the integrity and quality of clinical trial data. * Participate ...

New

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

Coordinate and manage assigned clinical trials from study start-up through completion. * Develop a ... Help ensure participant safety and the integrity and quality of clinical trial data. * Participate ...

New

Showing results 41-60

Clinical Research Data Manager information

See Rosharon, TX salary details

$43.8K

$96K

$169.1K

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

As of Aug 23, 2026, the average yearly pay for clinical research data manager in Rosharon, TX is $96,041.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $109,600.00 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 job categories do people searching Clinical Research Data Manager jobs in Rosharon, TX look for?

The top searched job categories for Clinical Research Data Manager jobs in Rosharon, TX are:

What cities near Rosharon, TX are hiring for Clinical Research Data Manager jobs?

Cities near Rosharon, TX with the most Clinical Research Data Manager job openings:

Infographic showing various Clinical Research Data Manager job openings in Rosharon, TX as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, 2% Temporary, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $96,041 per year, or $46.2 per hour.

Clinical Protocol Administration Manager - Pediatrics Research

MD Anderson Center

Houston, TX • On-site

Full-time

Medical, Dental, Retirement, PTO

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 891 rated healthcare providers


Job description

The Pediatrics Research department at MD Anderson Cancer Center is dedicated to advancing innovative clinical research that improves outcomes for children, adolescents, and young adults with cancer. Working in close collaboration with physicians, researchers, and multidisciplinary teams-including partners at Texas Children's Hospital-the department manages a robust portfolio of pediatric clinical trials designed to bring promising new therapies to patients. This collaborative research environment is committed to accelerating scientific discovery while ensuring the highest standards of patient safety, and operational excellence.
This Clinical Protocol Administration Manager position offers the opportunity to provide strategic and operational leadership for a growing pediatric clinical research program. The role is ideal for an experienced clinical research leader with a strong background in pediatric oncology research trials, who is passionate about building high-performing teams, optimizing research operations, and expanding access to innovative therapies for pediatric patients.
In this role, you will lead the administration and operational management of the pediatric clinical research portfolio by developing operational strategies, implementing standardized processes, monitoring key performance indicators, and driving initiatives that improve study activation, patient enrollment, operational efficiency, and research quality. You will collaborate with investigators, faculty, institutional leadership, and external partners to support strategic growth while developing dashboards, performance metrics, and operational reports that guide data-driven decision-making.
You will manage pediatric clinical research operations, oversee study execution while ensure compliance with institutional policies, Good Clinical Practice (GCP), sponsor requirements, and federal and state regulations. Responsibilities include workforce planning, staffing optimization, resource allocation, performance management, and operational oversight of clinical research personnel. As a key liaison between MD Anderson and Texas Children's Hospital, you will help align research priorities, standardize processes, and facilitate the successful execution of collaborative pediatric research initiatives.
A major component of this position is people leadership and professional development. You will recruit, mentor, coach, and develop clinical research staff while creating educational programs, competency assessments, cross-training initiatives, and career development opportunities that strengthen workforce capabilities and promote a culture of accountability, collaboration, and continuous learning.
You will also champion quality, compliance, and continuous improvement by overseeing quality assurance initiatives, preparing teams for sponsor audits, monitoring protocol compliance, implementing corrective and preventive action plans (CAPAs), evaluating quality metrics, and leading operational improvements that enhance research performance and regulatory readiness. Strong analytical skills, strategic thinking, and the ability to manage complex research operations are essential to success in this leadership role.
The ideal candidate will have progressive leadership experience in pediatric clinical research, with a strong background in pediatric oncology research. Experience managing research operations, leading multidisciplinary teams, and driving operational improvements within an academic medical center or comprehensive cancer center is highly preferred. Candidates who are passionate about advancing pediatric cancer research while developing high-performing research teams will find this opportunity especially rewarding.
MD Anderson offers a comprehensive total rewards package, including paid medical benefits, generous paid time off, retirement plans, tuition assistance, professional development opportunities, and additional benefits, along with the opportunity to build a rewarding leadership career at one of the world's leading cancer centers while helping shape the future of pediatric oncology research and bringing innovative therapies to children and young adults facing cancer.
**This position is hybrid and the exact details will be discussed more in the interview process**
JOB SPECIFIC COMPETENCIES
1. Administration and Management
Provides comprehensive planning, coordination, and operational support to advance the pediatric clinical research portfolio.
Develops and executes operational plans to support growth, sustainability, and performance of pediatric research programs.
Collaborates with faculty, investigators, team members, and external stakeholders to promote clinical trial development, enrollment growth, and research excellence.
Develops, implements, and evaluates policies, procedures, and operational standards to ensure efficient and effective research operations.
Establishes, monitors, and reports Key Performance Indicators (KPIs) related to clinical trials portfolio growth, patient accrual, study activation timelines, operational efficiency, workforce effectiveness, quality outcomes, regulatory compliance, and stakeholder satisfaction.
Leads initiatives to improve clinical trial access, enrollment performance, and operational effectiveness across pediatric research programs.
Develops operational dashboards and performance reporting mechanisms to support data driven decision making and resource allocation.
Identifies opportunities for process optimization and leads continuous improvement initiatives to enhance research productivity and reduce study activation timelines.
Collaborates with leadership on workforce planning, operational forecasting, resource allocation, and strategic initiatives that support organizational goals and clinical research portfolio growth.
2. Research Operations Management
Provides operational leadership and oversight for the successful execution of pediatric clinical research studies and programs.
Ensures compliance with institutional policies, sponsor requirements, federal and state regulations, Good Clinical Practice (GCP) standards, and applicable research guidelines.
Oversees operational performance of the pediatric clinical research portfolio and monitors achievement of enrollment, study activation, quality, and compliance objectives.
Evaluates clinical research performance metrics and trends to identify operational risks, opportunities, and corrective actions.
Maintains effective communication with investigators, clinical teams, regulatory personnel, and research stakeholders regarding ongoing and upcoming protocols.
Develops and manages staffing models, workforce planning strategies, and resource allocation processes to support research portfolio demands.
Provides leadership and supervision for pediatric clinical research personnel, including recruitment, onboarding, performance management, employee engagement, succession planning, and professional development.
Ensures effective resource utilization through staffing optimization, workload management, and cross-functional collaboration.
Implements best practices and standardized research processes to support operational consistency and program effectiveness.
Serves as an operational liaison between UT MD Anderson and Texas Children's Hospital to promote alignment of research priorities, standardization of processes, and successful execution of collaborative pediatric research initiatives.
3. Education, Training, Development and Mentoring
Identifies training and development needs and provides guidance on policies, procedures, and best practices related to clinical research operations and patient management.
Participates in the orientation, training, and ongoing professional development of pediatric clinical research personnel.
Plans, develops, and delivers educational programs, training sessions, presentations, and written communications to support protocol compliance and operational excellence.
Completes performance evaluations and provides coaching, mentoring, and feedback to personnel under direct supervision.
Develops workforce capability strategies that support organizational growth, employee engagement, and long-term operational excellence.
Establishes team development goals and monitors progress through competency assessments, certification attainment, training compliance, and career development planning.
Promotes a culture of accountability, collaboration, continuous learning, and professional growth.
Uses performance metrics, competency assessments, and employee feedback to identify development opportunities and implement targeted improvement plans.
Develops cross training programs to ensure operational continuity and workforce resilience.
Encourages team members' participation in professional organizations, educational activities, conferences, committees, and other career development opportunities.
4. Quality, Compliance and Continuous Improvement
Oversees quality assurance and quality improvement initiatives across pediatric clinical research operations.
Establishes quality and compliance standards and monitors performance through audits, protocol deviation reviews, corrective action plans, and quality assessments.
Leads operational readiness and preparation for internal, sponsor, regulatory, and external audits and inspections.
Monitors compliance with institutional, sponsor, federal, state, and Good Clinical Practice (GCP) requirements.
Develops and implements Corrective and Preventive Action plans (CAPAs) to mitigate compliance risks and improve operational effectiveness.
Reviews quality indicators, audit outcomes, performance metrics, and operational trends to drive continuous improvement and research excellence.
Identifies areas of risk and develop strategies that promote a culture of quality, accountability, and clinical compliance.
Performs other duties as assigned.
EDUCATION
Required: Bachelor's Degree Science, Healthcare, Nursing or related field.
Preferred: Master's Degree Science, Healthcare, Nursing or related field.
WORK EXPERIENCE
Required: 6 years Extensive research administrative experience in a biotechnology or academic setting to include two years experience with research protocols, grants and contracts and 2 years Supervisory/management experience.
May substitute additional experience for required education (or vice versa) on a one to one year basis.
Successful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience. Completion of both programs can be substituted for a maximum of two years of supervisory or management experience.
OTHER REQUIREMENTS: Must pass pre-employment skills test as required and administered by Human Resources.
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

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