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Study Manager Jobs in Texas (NOW HIRING)

ICF

Senior Transmission Planning Engineer

Dallas, TX · On-site

$103K - $142K/yr

Serve as technical lead or study manager on transmission planning engagements, owning scope, schedule, quality, and client relationship * Perform steady-state load flow and contingency analysis (PSS ...

Medpace, Inc.

Study Start-Up Project Manager

Irving, TX · On-site +1

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...

Medpace, Inc.

Study Start-Up Project Manager

Irving, TX · On-site

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...

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Study Manager information

See Texas salary details

$22.8K

$55.5K

$108.1K

How much do study manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for study manager in Texas is $55,457.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,100.00 and $63,800.00 per year, depending on experience, location, and employer.

How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What are the key skills and qualifications needed to thrive as a study manager?

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What does a study manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
What are the most commonly searched types of Study jobs in Texas? The most popular types of Study jobs in Texas are:
What cities in Texas are hiring for Study Manager jobs? Cities in Texas with the most Study Manager job openings:
Study Manager jobs near you
Infographic showing various Study Manager job openings in Texas as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $55,457 per year, or $26.7 per hour.

Clinical Research Coordinator - Project Hire

Senseye

Austin, TX • On-site

$24 - $32/hr

Full-time

Re-posted 2 days ago

Job description

About Us
Senseye is a NeuroTechnology Company in Austin, TX, on the cusp of revolutionizing Mental Health. Over the past six years, we have invested millions of dollars in R&D to build our platform, allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases, we are now focused on building the world's first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform that gives clinicians a safe and objective, accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for millions of sufferers. The Senseye platform could be the technology that drives this change. This is an excellent opportunity to shape the future of digital medicine and address unmet medical needs that affect billions of people worldwide.
What we are looking for:
This is a fixed-term project position expected to continue through the completion of our Phase III trial. Team members who demonstrate strong performance and align with our long-term needs may be considered for permanent opportunities as the organization continues to grow. The anticipated duration of the project is expected to be between 6-12 months.
The Research Coordinator is primarily responsible for recruiting, qualifying, and consenting experimental participants, running participants through experiments, organizing experiment logistics, and maintaining data records per Good Clinical Practices. We are looking for a candidate eager to grow into a clinical research supervisory role.
Responsibilities
  • Adhere to the IRB-approved protocol and coordinate protocol-related research procedures, study visits, and follow-up care, ensuring the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA, and all required obligations to patient/subject, Principal Investigator, Research Team and sponsor, and other appropriate agencies
  • The Clinical Research Coordinator is an active participant in all study components from research planning to study completion, including direct involvement in case management of study participants, study coordination, and data collection to ensure compliance in study conduct and adherence to the study protocol
  • Participates in pre-screening and recruitment activities to identify patients who may be eligible for research study participation
  • Run participants through experiments and record study data per the clinical study protocol. Ensure the participant has a positive experience and that high-quality data is collected. Share feedback from participants to help improve the participant experience.
  • Function as liaison between research sites, clinicians, participants, and other internal and external stakeholders
  • Maintain accurate data records, and maintain a follow-up calendar, ensuring all follow-up assessments are completed per protocol.
  • Own study progress and updates in team project management software
  • Proactively alert the study manager and study team of issues that may arise
  • Manage and respond to project-related email and phone inquiries. Maintain effective communication with research participants when engaging in participant recruitment, enrollment, tracking, retention, and data collection.
  • Data entry (e.g., transferring study data from paper forms to the electronic database)
  • Prepare, maintain, and update technical documentation
  • Attend weekly project meetings
  • Coordinate with the research team, clinicians, and engineering to ensure project success
  • Any other duties needed to help drive our vision, fulfill our mission, and abide by our organization's values

Extra Points:
  • Experienced clinical research coordinator
  • Experience with patients with psychiatric disorders is a plus
  • Organized and detail-oriented, with the ability to multitask
  • Self-starter and quick learner

Requirements
  • We are open to a range of education and work experiences for this role. Familiarity with research studies and tabular data is preferred, but no degree is specified.
  • Excellent attention to detail
  • Strong interest in clinical research
  • Prior laboratory or human subjects research experience
  • Professional demeanor, especially when interacting with participants
  • Strong organizational skills and interpersonal skills

Benefits
  • The anticipated duration of the position is less than one year, this role is not initially eligible for company-sponsored benefits. Should the position extend beyond one year, benefit eligibility will be determined in accordance with the Company's benefit plans and eligibility requirements in effect at that time.
  • This position follows a hybrid work schedule. Employees are expected to work in the office on a regular basis and may work remotely as approved by their manager and based on business needs.
  • Commuter benefits for parking, public transit, carshares, etc.
  • Fully stocked kitchen
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About Senseye

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

11 - 50 Employees

Headquarters location

Austin, TX, US

Year founded

2015

Social media

Twitter

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