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Clinical Trial Manager Jobs in Spring, TX (NOW HIRING)

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 ...

A Study Manager I is responsible to ensure that quality research is conducted at assigned ... Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

The primary purpose of the Clinical Trial Technician position is to support the execution of clinical trials by collecting, processing, and managing biological specimens, maintaining laboratory ...

The primary purpose of the Clinical Trial Technician position is to support the execution of clinical trials by collecting, processing, and managing biological specimens, maintaining laboratory ...

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

The primary purpose of the Clinical Trial Technician position is to support the execution of clinical trials by collecting, processing, and managing biological specimens, maintaining laboratory ...

The primary purpose of the Clinical Trial Technician position is to support the execution of clinical trials by collecting, processing, and managing biological specimens, maintaining laboratory ...

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Clinical Trial Manager information

See Spring, TX salary details

$25

$55

$85

How much do clinical trial manager jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for clinical trial manager in Spring, TX is $55.63, according to ZipRecruiter salary data. Most workers in this role earn between $45.14 and $62.69 per hour, depending on experience, location, and employer.

What does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

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

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

What are the most commonly searched types of Clinical Trial jobs in Spring, TX?

The most popular types of Clinical Trial jobs in Spring, TX are:

What are popular job titles related to Clinical Trial Manager jobs in Spring, TX?

For Clinical Trial Manager jobs in Spring, TX, the most frequently searched job titles are:

What cities near Spring, TX are hiring for Clinical Trial Manager jobs?

Cities near Spring, TX with the most Clinical Trial Manager job openings:

Infographic showing various Clinical Trial Manager job openings in Spring, TX as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $115,716 per year, or $55.6 per hour.

Clinical Trial Screening Coordinator

DM Clinical Research

Tomball, TX

Full-time

Re-posted yesterday


Job description

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 amp; 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 amp; 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:
  • Dependability
  • 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