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Clinical Trial Program Manager Jobs in Texas (NOW HIRING)

IQVIA

Clinical Trial Rater

Houston, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

IQVIA

Clinical Trial Rater

Dallas, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

MD Anderson

Clinical Trial Laboratory Coordinator

Houston, TX · Hybrid

$34.62 - $41.59/hr

... programs. Responsibilities Trial Management & Stakeholder Collaboration Lead protocol execution ... Clinical Trial Inventory & Service Coordination Maintain and track clinical trial kit inventory to ...

New

MD Anderson

Clinical Trial Laboratory Coordinator

Houston, TX · Hybrid

$34.62 - $41.59/hr

... programs. Responsibilities Trial Management & Stakeholder Collaboration • Lead protocol execution, conduct quality assurance audits, participate in monitor visits, and maintain protocol integrity ...

New

Lumiresearch

PRN - Clinical Trial PharmD

Houston, TX · On-site

$100 - $130/hr

The primary purpose of the Clinical Trial PharmD is to provide oversight for investigational drug ... Oversee investigational product (IP) management, including receipt, storage, temperature monitoring ...

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Clinical Trial Program Manager information

What does a clinical trial program manager do?

A Clinical Trial Program Manager oversees the planning, execution, and completion of clinical trials within an organization. They coordinate cross-functional teams, manage timelines and budgets, ensure compliance with regulatory guidelines, and maintain the quality and integrity of clinical data. Their role is essential for the successful development of new medical treatments, as they bridge communication between stakeholders, monitor progress, and address any issues that arise during trials.

What are some common challenges faced by clinical trial program managers, and how can they be addressed?

Clinical Trial Program Managers often encounter challenges such as managing complex timelines, coordinating multiple stakeholders, and ensuring regulatory compliance across different study sites. These challenges can be addressed by implementing robust project management tools, maintaining clear and consistent communication with cross-functional teams, and staying updated on regulatory requirements. Developing strong organizational skills and fostering collaborative relationships with investigators, sponsors, and regulatory bodies are also key to overcoming obstacles in this role.

What are the key skills and qualifications needed to thrive as a clinical trial program manager, and why are they important?

To thrive as a Clinical Trial Program Manager, you need strong project management skills, a background in life sciences or healthcare, and experience with clinical research regulations such as GCP, often supported by a relevant degree and certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory submission tools is typically required. Exceptional leadership, communication, and problem-solving abilities help you coordinate teams and manage complex stakeholder relationships. These skills ensure that clinical trials are conducted efficiently, compliantly, and successfully, leading to reliable study outcomes and regulatory approval.

What are popular job titles related to Clinical Trial Program Manager jobs in Texas?

For Clinical Trial Program Manager jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Program Manager jobs in Texas look for?

The top searched job categories for Clinical Trial Program Manager jobs in Texas are:

What cities in Texas are hiring for Clinical Trial Program Manager jobs?

Cities in Texas with the most Clinical Trial Program Manager job openings:

Clinical Trial Program Manager jobs near you
Infographic showing various Clinical Trial Program Manager job openings in Texas as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Clinical Trial Screening Coordinator

DM Clinical Research

Tomball, TX • On-site

$50 - $70/hr

Other

Re-posted 5 days ago

Job description

Position: Clinical Trial Screening Coordinator

Location: Tomball, TX

Job Id: 1102

# of Openings: 1

Clinical Trial Screening Coordinator

The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are assigned to the trial best suited for them. To ensure that subjects have the required paperwork, medical records, and authorizations to participate in trials. To demonstrate effective knowledge of protocols, including inclusion/exclusion criteria. To demonstrate knowledge of Good Clinical Practices and FDA regulations specifically pertaining to the recruitment and retention of study subjects.

DUTIES & RESPONSIBILITIES
  • Completing DMCR-required training, including GCP and NIH.
  • Ensuring all patient enrollment activities are performed as per clinical trial protocol parameters by engaging directly with the CRCs and working closely with the clinical trial team.
  • Interfacing with potential research subjects to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent and coordinate appointments with the recruitment team.
  • Managing pre-screen operational activities and establishing strong relationships with clinical trial sites and the staff.
  • Accountable for coordinating pre-screen data management activities - performing quality checks on timely data entry and data quality in the clinical research electronic system (CRIO).
  • Ensuring availability of study participant's information by accurately filing and/or retrieving study participant records as requested by management
  • Being prepared for and available at all required company meetings.
  • Submitting administrative paperwork per company timelines.
  • Any other matters as assigned by management.
KNOWLEDGE & EXPERIENCE Education
  • FMG (Foreign Medical Graduate) preferred or
  • Bachelors in Health Care Sciences or
  • Nursing Degree- LVN, LPN, or RN
Experience
  • 3-4 years of Medical terminology
  • 1-2 years of customer service experience
  • 1-2 years of clinical research experience preferred
Credentials
  • N/A
Knowledge and Skills
  • Medical Spanish a plus
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have attention to detail and accuracy.
  • Extreme attention to detail (strict adherence to procedures and protocols is essential)
  • Good knowledge of Good Clinical Practices and FDA regulations, protocols
  • Ability to use computer applications for data capture and for general communication required to
  • Communicate effectively, both orally and in writing
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