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Study Director Jobs in Houston, TX (NOW HIRING)

A Study Manager I is responsible to ensure that quality research is conducted at assigned ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...

Study Manager I

Houston, TX · On-site

$100 - $125/hr

Assist the Associate Site Director/Site Director with staff training and any other relevant tasks ... study protocols and ensure patients' understanding before obtaining their consentFacilitate ...

Study Manager I

Sugar Land, TX · On-site

$80 - $100/hr

Assist the Associate Site Director/Site Director with staff training and any other relevant tasks ... study protocols and ensure patients' understanding before obtaining their consentFacilitate ...

A Study Manager I is responsible to ensure that quality research is conducted at assigned ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...

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Study Director information

See Houston, TX salary details

$43K

$122.6K

$222K

How much do study director jobs pay per year?

As of Sep 7, 2026, the average yearly pay for study director in Houston, TX is $122,587.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,400.00 and $180,000.00 per year, depending on experience, location, and employer.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

What are the most commonly searched types of Study jobs in Houston, TX?

The most popular types of Study jobs in Houston, TX are:

What are popular job titles related to Study Director jobs in Houston, TX?

For Study Director jobs in Houston, TX, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in Houston, TX look for?

The top searched job categories for Study Director jobs in Houston, TX are:

What cities near Houston, TX are hiring for Study Director jobs?

Cities near Houston, TX with the most Study Director job openings:

Infographic showing various Study Director job openings in Houston, TX as of August 2026, with employment types broken down into 2% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $122,587 per year, or $58.9 per hour.

Research Scientist I - Ophthalmology

UTMB Health

Galveston, TX • On-site

Full-time

Re-posted 12 days ago


UTMB Health rating

7.2

Company rating: 7.2 out of 10

Based on 172 frontline employees who took The Breakroom Quiz

346th of 898 rated healthcare providers


Job description

MINIMUM QUALIFICATIONS: 

Ph.D. and/or MD, DVM.  1 - 3 years of experience conducting regulated studies.  7+ years of experience in infectious diseases research with viral or bacterial pathogens, including animal studies.  Good Laboratory Practice training.  BSL3 and/or BSL4 laboratory training.  Experience with qualitative data collection and analysis including mixed method approaches.  Able to obtain clearance for work with Tier 1 Select Agents and be registered as a Principal Investigator under the US Federal Select Agent Program (FSAP).

JOB SUMMARY

Function: The Regulatory Scientist II will be assigned as a Study Director, as defined by the U.S. FDA Good Laboratory Practice (GLP) regulations (21CFR58), and will serve as the single point of study control with overall responsibility for the scientific, technical and regulatory conduct of studies as well as for the interpretation, documentation and reporting of results.  The Regulatory Scientist II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies (ORNcS), study sponsors and/or funding agencies to design and execute regulated nonclinical studies compliant with the U.S. FDA GLP regulations or under quality systems that utilize the US FDA GLP regulations as a reference standard.  The Regulatory Scientist II may also function as a Principal Investigator for extramurally funded research programs and be expected to manage complex programs with multiple studies. 

ESSENTIAL JOB FUNCTIONS:

  • Conduct innovative scientific investigations by developing theories and devising scientific methods and procedures to apply scientific principles, theories, and research in projects related to the mission of UTMB. Participate in the discovery of new innovative biomedical and health services knowledge leading to increasingly effective and accessible health care for the citizens of Texas.  
  • Manage computational laboratory operations, including staff development and adherence to applicable policies, laws, and regulations. 
  • Establishes research objectives and methodology, designs procedures, conducts research projects, analyzes, and interprets results.
  • Preparation and publication of manuscripts in peer review journals.
  • Ensures proper training of Research staff, Pre and Post-Doctoral Fellows.
  • Adheres to internal controls and reporting structure
  • Algorithm development and performance optimization
  • Big data analytics
  • Data engineering
  • Statistical analysis
  • Data visualization
  • Data mining and machine learning 
  • Network analysis
  • Ability to manage research projects with minimal supervision
  • Bioinformatics tools and databases
  • Writing and presentation skills
  • Problem solving and creativity

USEFUL SKILLS/EXPERIENCE WITH: 

  • Cell culture
  • Molecular biology

SALARY:
Commensurate with experience

Equal Employment Opportunity

UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.

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