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Clinical Research Program Manager Jobs in Texas (NOW HIRING)

Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

The CRA will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical research timeline from pre-site ...

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Clinical Research Program Manager information

See Texas salary details

$41.5K

$86.3K

$139.3K

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

As of Aug 7, 2026, the average yearly pay for clinical research program manager in Texas is $86,274.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $97,800.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.
What are popular job titles related to Clinical Research Program Manager jobs in Texas? For Clinical Research Program Manager jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Research Program Manager jobs in Texas look for? The top searched job categories for Clinical Research Program Manager jobs in Texas are:
What cities in Texas are hiring for Clinical Research Program Manager jobs? Cities in Texas with the most Clinical Research Program Manager job openings:
Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $86,274 per year, or $41.5 per hour.

Senior Coordinator, Clinical Research Program (Regulatory) - Leukemia

MD Anderson Center

Houston, TX • On-site

$32.21 - $40.14/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

MD Anderson Cancer Center rating

8.4

Company rating: 8.4 out of 10

Based on 170 frontline employees who took The Breakroom Quiz

24th of 887 rated healthcare providers

Job description

Senior Coordinator, Clinical Research Program - Leukemia
The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Clinical Research Program Clinical Research Program supports the advancement of clinical research within the Leukemia program by coordinating complex regulatory, administrative, financial, and operational activities associated with clinical trials.
The Clinical Research Program Senior Coordinator serves as a key resource for investigators, sponsors, and research teams to ensure protocol compliance, study activation, and successful trial execution. They contribute to the delivery of high-quality clinical research that supports UT MD Anderson's mission to eliminate cancer through exceptional programs in patient care, research, education, and prevention.
The ideal candidate will possess a Master's degree in Nursing, Public Health, Healthcare Administration, or a related scientific field, along with significant experience in research studies, clinical research administration, direct patient care, nursing, data gathering, or a related field. Candidates with experience managing regulatory submissions, protocol development, investigator support, clinical trial start-up activities, sponsor collaboration, compliance oversight, and clinical research operations will be well suited for this role.
Hourly Salary Range (40-hour work week): Minimum $32.21 - Midpoint $40.14 - Maximum $48.08
Work Location: Remote
Why Us?
This role offers the opportunity to support innovative leukemia clinical research while collaborating with multidisciplinary teams, investigators, sponsors, and research professionals. The position plays a critical role in advancing research that impacts patient outcomes while providing opportunities for professional growth, continued learning, and meaningful contributions to UT MD Anderson's mission.
  • 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
Administrative & Regulatory Operations
  • Manage administrative and regulatory aspects of federal and pharmaceutical-funded research protocols through all study phases
  • Provide administrative support to Principal Investigators for study development, implementation, and completion
  • Independently prepare protocol documents that comply with regulatory and institutional requirements
  • Collaborate with sponsors and Clinical Research Organizations to develop budget documents meeting institutional and sponsor requirements
  • Submit protocols for Clinical Research Committee and Institutional Review Board review
  • Respond on behalf of Principal Investigators to reviewer comments when appropriate
  • Coordinate site start-up activities and oversee overall financial trial management
  • Assist with preparation of responses to Clinical Research Committee and Institutional Review Board reviews
  • Serve as liaison with pharmaceutical sponsors regarding informed consent document language
  • Develop and maintain tracking systems, status reports, regulatory files, and organizational records for clinical trials

Clinical Trial Integrity & Program Support
  • Review protocols, amendments, and ancillary documents to identify discrepancies and clarify requirements
  • Collaborate with investigators and sponsors to resolve protocol-related issues
  • Prepare and submit reports to sponsors, investigators, regulatory authorities, and management
  • Support strategic and long-range planning for departmental clinical trial programs
  • Coordinate weekly clinical research review meetings and ad hoc protocol review meetings
  • Partner with clinical faculty to support departmental clinical trial goals
  • Ensure all protocol reviews are addressed to the satisfaction of reviewers
  • Manage new protocol start-up processes and study activation requirements

Training, Compliance & Education
  • Attend training related to clinical trial documentation, regulatory requirements, and departmental procedures
  • Maintain compliance with Good Clinical Research Practice standards
  • Create presentations and visual aids addressing regulatory aspects of clinical research administration
  • Assist with educational programs and in-service training for faculty and staff
  • Communicate regulatory and protocol-related updates to team members
  • Participate in the development of departmental clinical research policies and procedures
  • Support development of in-service educational events for team members
  • Maintain current knowledge of clinical trial processes and regulatory requirements
  • Orient new faculty and support personnel to clinical research infrastructure and procedures

Laboratory & Protocol Management
  • Monitor protocol start-up activities and ensure laboratory personnel understand assigned responsibilities
  • Participate in site initiation visits to clarify sample collection, processing, and shipment requirements
  • Create study collection sheets according to protocol specifications
  • Submit and manage protocol amendments, updates, and regulatory documentation
  • Coordinate protocol implementation activities between investigators, laboratories, and research teams

Information Systems & Reporting
  • Develop and maintain processing and tracking systems for protocol-related documentation
  • Establish and participate in systems supporting protocol development, submission, processing, and maintenance
  • Generate monthly, quarterly, and annual productivity and responsiveness reports
  • Provide protocol-related information and data for grant applications
  • Manage clinical trial-related grant applications through public and private funding mechanisms
  • Collaborate on departmental grant applications as a preparation and production

EDUCATION
  • Required: Bachelor's Degree
  • Preferred: Master's Degree Nursing, Public Health, Healthcare Administration or related scientific field.

WORK EXPERIENCE
  • Required: Five years experience in research study or direct patient care obtained from nursing, data gathering or related field or three years required experience with preferred degree.
  • May substitute required education degree with additional years of equivalent experience on a one-to-one basis.

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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