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Clinical Research Operations Jobs in Texas (NOW HIRING)

Guided by our core values--Scientific Rigor, Operational Excellence, Commitment to Sponsors and ... Overview Adams Clinical is a rapidly growing research site network specializing focused on late ...

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

Guided by our core values-Scientific Rigor, Operational Excellence, Commitment to Sponsors and ... Overview Adams Clinical is a rapidly growing research site network specializing focused on late ...

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

Guided by our core values-Scientific Rigor, Operational Excellence, Commitment to Sponsors and ... Overview Adams Clinical is a rapidly growing research site network specializing focused on late ...

Clinical Research Coordinator Location: Multiple Locations - TX, VA, FL Employment Type: Contract ... Coordinate routine operational activities across multiple research protocols * Serve as a liaison ...

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Clinical Research Operations information

See Texas salary details

$45.7K

$100K

$176.1K

How much do clinical research operations jobs pay per year?

As of Aug 25, 2026, the average yearly pay for clinical research operations in Texas is $100,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $114,100.00 per year, depending on experience, location, and employer.

What is clinical research operations?

Clinical research operations refer to the planning, execution, and management of clinical trials and studies that test new medical treatments, drugs, or devices. This field ensures that studies are conducted ethically, efficiently, and in compliance with regulatory guidelines. Professionals in clinical research operations coordinate activities such as patient recruitment, data collection, regulatory submissions, and quality control. Their work is essential for advancing medical knowledge and ensuring the safety and effectiveness of new healthcare interventions.

What are the key skills and qualifications needed to thrive in clinical research operations?

To thrive in Clinical Research Operations, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as ICH-GCP), and project management, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are often required. Exceptional organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring compliance. These competencies are vital for maintaining data integrity, meeting regulatory standards, and successfully managing complex clinical studies.

What are some common challenges faced in clinical research operations and how can they be addressed?

Professionals in clinical research operations often encounter challenges such as managing complex regulatory requirements, coordinating across multidisciplinary teams, and ensuring adherence to strict timelines. Successfully addressing these challenges typically involves strong project management skills, effective communication with stakeholders, and staying updated on regulatory changes. Leveraging technology for data management and fostering a collaborative work environment can also help streamline processes and improve trial outcomes.

What is the difference between Clinical Research Operations vs Clinical Research Coordinators?

AspectClinical Research OperationsClinical Research Coordinators
CredentialsTypically requires a degree in life sciences, certifications like CCRP or RACOften requires a bachelor's degree in health sciences or related field, with certifications like CCRP beneficial
Work EnvironmentOversees multiple studies, manages teams, and collaborates with sponsors and regulatory bodiesWorks directly with study participants, manages data collection, and ensures protocol adherence
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutionsCommonly employed in hospitals, clinics, and research sites

Clinical Research Operations professionals focus on managing entire research programs, budgets, and teams, while Clinical Research Coordinators handle day-to-day study activities and participant interactions. Both roles are essential but differ in scope and responsibilities within the clinical research field.

Is clinical research operations a good career?

Clinical research operations involves managing and coordinating clinical trials to ensure they meet regulatory standards and are completed efficiently. It offers opportunities for growth, requires strong organizational and communication skills, and often involves working with cross-functional teams and specialized software. Many professionals find it a rewarding field with stable employment prospects in the healthcare and pharmaceutical industries.

What are the most commonly searched types of Clinical Research Operations jobs in Texas?

The most popular types of Clinical Research Operations jobs in Texas are:

What are popular job titles related to Clinical Research Operations jobs in Texas?

For Clinical Research Operations jobs in Texas, the most frequently searched job titles are:

Infographic showing various Clinical Research Operations job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $100,000 per year, or $48.1 per hour.

Clinical Protocol Administration Manager - Pediatrics Research

MD Anderson

Houston, TX • Hybrid

Full-time

Medical, Dental, Retirement, PTO

Posted 15 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 893 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 Additional Information Requisition ID: 182366 Employment Status: Full-Time Employee Status: Regular Work Week: Days Minimum Salary: US Dollar (USD) 95,000 Midpoint Salary: US Dollar (USD) 118,500 Maximum Salary : US Dollar (USD) 142,000 FLSA: exempt and not eligible for overtime pay Fund Type: Soft Work Location: Onsite Pivotal Position: Yes Referral Bonus Available?: Yes Relocation Assistance Available?: Yes #LI-Onsite Apply


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