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Clinical Research Program Manager Jobs in Manvel, TX

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Clinical Research Coordinator II

Pasadena, TX

$20.75 - $27.50/hr

The Clinical Research Coordinator II leads the clinical research program at the site level ... Ongoing Study oversight and management: * Plan subject visits according to protocol specific visit ...

Care Access

Clinical Research Assistant

Houston, TX

$19 - $33/hr

With programs like Future of Medicine , which makes advanced health screenings and research ... and management.  * Communicate clearly verbally and in writing.  * Participate in ...

FOCUSPOINT

Clinical Research Coordinator

Webster, TX · On-site

Clinical Research Coordinator Location: Multiple Locations - TX, VA, FL Employment Type: Contract ... Manage study timelines from feasibility through study closeout * Review study criteria with ...

Care Access

Clinical Research Assistant

Houston, TX · On-site

$19 - $33/hr

With programs like Future of Medicine, which makes advanced health screenings and research ... personnel and management. * Communicate clearly verbally and in writing. * Participate in ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Manvel, TX

Clinical Research Program Manager information

See Manvel, TX salary details

$41.9K

$87.1K

$140.6K

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

As of Jul 27, 2026, the average yearly pay for clinical research program manager in Manvel, TX is $87,120.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,200.00 and $98,800.00 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, and why are they important?

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 Manvel, TX? For Clinical Research Program Manager jobs in Manvel, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Research Program Manager jobs in Manvel, TX look for? The top searched job categories for Clinical Research Program Manager jobs in Manvel, TX are:
What cities near Manvel, TX are hiring for Clinical Research Program Manager jobs? Cities near Manvel, TX 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 Manvel, TX as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 19% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $87,120 per year, or $41.9 per hour.

Clinical Research Coordinator

Shrinerschildrens

Galveston, TX

$26.58 - $39.86/hr

Full-time

Posted 16 days ago

Job description

Company Overview

Shriners Children's is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family's ability to pay or insurance status. Please click here to learn more about our locations.

Job Description

The Clinical Research Coordinator, Level 1 (CRC I)is a research professional responsible for supporting the oversight and compliance of both system-wide and local Shriners Children's (SHC) clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and collaborating with the Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice (GCP) guidelines, when applicable.

The CRC works collaboratively with investigators, research staff, and clinical teams to ethically recruit and consent Shriners Children's vulnerable pediatric research participants and to appropriately collect, manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and the quality and integrity of study data.

Key Responsibilities:

  • Supports the implementation and conduct of approved research protocols, ensuring studies are performed in compliance with the protocol, Good Clinical Practice (GCP), applicable regulatory requirements, and SHC policies and standards.

  • Performs study-specific research activities and/or interventions within the bounds of professional licensure and training.

  • Assists with participant recruitment, screening, informed consent/assent, scheduling, and coordination of study visits.

  • Coordinates the collection and documentation of research data.

  • Maintains regulatory documentation and study records in accordance with institutional policies and sponsor requirements.

  • Supports communication and coordination between investigators, sponsors, monitors, and institutional departments involved in research activities.

  • Assists investigators with the development and submission of investigator-initiated research protocols and related regulatory documentation.

  • Contributes to study progress reports, monitoring visits, audits, and preparation of study results or presentations when applicable.

  • Ensures appropriate training and education are completed in order to safely perform study-related procedures and protocol requirements.

Required Qualifications:

  • 1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)

Preferred Qualifications:

  • Bachelor's degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field

  • Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)

  • Experience coordinating intergroup or multi-site clinical studies

  • CCRP or CCRC certification

The pay range for this position is $26.58 - $39.86. Compensation is determined based on years of relevant experience and departmental equity.

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