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Study Director Jobs in Texas (NOW HIRING)

RPM ReSearch

Study Director II

Corpus Christi, TX

$80K - $110K/yr

Study Director - Non-Human Primate Research Program Location: Corpus Christi, Texas Job Type: Full-Time About the Opportunity Are you an experienced Study Director with a passion for in-vivo research ...

Neuralink

Preclinical Study Coordinator

Austin, TX · On-site

Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...

Neuralink

Preclinical Study Coordinator

Austin, TX · On-site

$31 - $53/hr

Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...

DM Clinical

Study Manager I (4011)

Sugar Land, TX · On-site

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 ...

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Required Experience * 2+ years of global study management experience * Experience across multiple ... Make a direct impact on patient outcomes worldwide IQVIA is a leading global provider of clinical ...

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Study Director information

See Texas salary details

$41.9K

$119.6K

$216.6K

How much do study director jobs pay per year?

As of Aug 6, 2026, the average yearly pay for study director in Texas is $119,594.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $175,600.00 per year, depending on experience, location, and employer.

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 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.

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 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.

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.
More about Study Director jobs
What are the most commonly searched types of Study jobs in Texas? The most popular types of Study jobs in Texas are:
What are popular job titles related to Study Director jobs in Texas? For Study Director jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Study Director jobs in Texas look for? The top searched job categories for Study Director jobs in Texas are:
What cities in Texas are hiring for Study Director jobs? Cities in Texas with the most Study Director job openings:
Study Director jobs near you
Infographic showing various Study Director job openings in Texas as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $119,594 per year, or $57.5 per hour.

Study Director II

RPM ReSearch

Corpus Christi, TX

$80K - $110K/yr

Full-time

Re-posted 10 days ago

Job description

Study Director – Non-Human Primate Research Program

Location: Corpus Christi, Texas


Job Type: Full-Time


About the Opportunity

Are you an experienced Study Director with a passion for in-vivo research and NHP (non-human primate) studies? Join our expanding research program as we build upon our existing infrastructure and create new capabilities within a collaborative, multi-site organization.

Our facility is entering an exciting phase of growth, adding innovative programs and resources to support cutting-edge biomedical research. As part of a national network of research sites, you'll have access to a broad community of experts, opportunities for cross-site collaboration, and continuous professional growth.


Key Responsibilities


Study Planning & Execution:

  • Oversee all phases of assigned studies, including protocol development, resource planning (animals and personnel), and scheduling to ensure alignment with SOPs and sponsor expectations.

Sponsor Communication:

  • Serve as the primary point of contact for study sponsors, maintaining regular, proactive communication throughout the project lifecycle.

Protocol & Compliance Oversight:

  • Draft, review, and obtain approvals for study protocols. Ensure compliance with internal SOPs, USDA regulations, the Animal Welfare Act, IACUC requirements, and the Guide for the Care and Use of Laboratory Animals.

Data & Quality Management:

  • Review and approve data collection forms, formulation instructions, and labels. Verify that all experimental data is recorded accurately and promptly address deviations or unexpected events.

Reporting & Documentation:

  • Compile and submit study results in collaboration with senior staff and principal investigators. Ensure data and specimen archiving or transfer aligns with organizational standards and sponsor requirements.

Training & Supervision:

  • Identify special methods and ensure technical staff receive appropriate training. Provide mentorship and guidance as needed.

Operational Support:

  • Be available for extended hours, holidays, and weekends as required. Support facility-wide safety and PPE compliance efforts.


Qualifications


  • Bachelor’s degree in a scientific discipline (e.g., Biology, Pharmacology, or related field).
  • 3–5 years of experience in in-vivo study execution or direction, preferably in pharmacology, pharmacokinetics, or toxicology.
  • Experience managing NHP studies is highly preferred.
  • Strong communication and organizational skills with an emphasis on sponsor-facing roles.
  • Familiarity with GLP/GCP environments is an asset, however, at this time the facility is not conducting GLP studies
  • Comfortable using digital data systems and troubleshooting common issues.


Why Join Us?


  • Innovative Environment: Be part of a growing research program focused on NHP studies.
  • Collaborative Culture: Network with professionals across multiple U.S. research sites.
  • Career Development: Access leadership support and training opportunities as the program scales.
  • Meaningful Work: Contribute to impactful biomedical research that advances health and science.


Ready to take the next step in your research leadership career?

Let's talk and help shape the future of translational research.