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Clinical Research Program Manager Jobs in Texas (NOW HIRING)

Adams Clinical

Clinical Research Assistant

Dallas, TX

$19.23 - $23.08/hr

Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Employee assistance program * Flexible spending account * Health insurance * Health savings account

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Texas

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.

Clinical Research Coordinator - Onsite

Advanced Rheumatology of Houston

The Woodlands, TX • On-site

$40K - $75K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 12 days ago

Job description

Experienced Clinical Research Coordinator – Rheumatology
Location: The Woodlands, Texas
Position Type: Full-Time
Work Arrangement: Onsite only — this is not a remote position.
Advance Your Clinical Research Career With a Growing Rheumatology Practice

Are you an experienced Clinical Research Coordinator who is passionate about improving patient care and contributing to meaningful medical advancements?
Our growing private rheumatology practice in The Woodlands, Texas, is seeking a motivated and highly organized Clinical Research Coordinator (CRC) to join our research team. In this hands-on role, you will help coordinate clinical trials involving autoimmune, inflammatory, and rheumatologic conditions while working closely with patients, investigators, sponsors, and clinical research partners.
This opportunity is ideal for a detail-oriented research professional who thrives in a fast-paced clinical environment, enjoys building relationships with patients, and takes pride in maintaining high standards of quality, compliance, and documentation.
Key Responsibilities:
  • Coordinate clinical trials from study startup through closeout.
  • Identify, screen, recruit, and consent eligible research participants.
  • Coordinate and conduct study visits, including patient education and follow-up.
  • Ensure all study activities are completed according to the protocol, Good Clinical Practice guidelines, FDA regulations, and site procedures.
  • Collect, document, and maintain accurate source documentation and study data.
  • Manage study schedules, visit windows, deadlines, and required follow-up activities.
  • Maintain regulatory binders, IRB submissions, essential documents, and study correspondence.
  • Serve as a primary point of contact for investigators, sponsors, CROs, monitors, and regulatory representatives.
  • Prepare for and assist with monitoring visits, audits, inspections, and study closeout activities.
  • Respond to data queries and help ensure study records are complete, accurate, and audit-ready.
  • Collaborate with clinical and research staff to provide a positive experience for study participants.
  • Process and ship biological specimens.

Qualifications:
  • A minimum of 1 year of clinical research coordination experience is required.
  • Experience with rheumatology, autoimmune diseases, or inflammatory-condition studies is strongly preferred.
  • Strong knowledge of Good Clinical Practice, FDA regulations, informed consent requirements, and clinical trial processes.
  • Demonstrated ability to manage multiple studies, competing priorities, and deadlines.
  • Excellent organizational, communication, documentation, and patient-interaction skills.
  • Ability to work independently while contributing to a collaborative team environment.
  • Proficiency with electronic medical records, electronic data capture systems, and clinical trial management software.
  • CCRC, CCRP, or an equivalent clinical research certification is preferred but not required.
  • Nursing or other direct clinical experience is a plus.
  • Experience performing blood draws, processing specimens, and preparing laboratory samples for shipment is preferred.
  • Fluency in Spanish is preferred.
  • Must be available to work onsite at our location in The Woodlands, Texas. Remote work is not available for this position.

What We Offer:
  • Competitive compensation based on experience.
  • Health, dental, and vision insurance.
  • Paid time off and paid holidays.
  • A supportive, collaborative, and patient-centered work environment.
  • The opportunity to work with an experienced rheumatology and clinical research team.
  • Professional growth opportunities within a growing research program.
  • The chance to contribute directly to advancements in treatments for autoimmune and rheumatologic conditions.

Join Our Team
Become part of a dedicated team committed to conducting high-quality clinical research and improving outcomes for patients living with autoimmune and inflammatory conditions. This is an exciting opportunity to use your research experience in a respected private-practice setting where your work will have a meaningful impact.