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Study Manager Jobs in Texas (NOW HIRING)

Houston Methodist

Manages study quality assurance and actively participates in quality assurance program for research studies. Proactively plans for routine events in research and anticipates/prevents and manages ...

SGS

Clinical Study Project Manager

Richardson, TX · On-site

The Study Project Manager is ultimately accountable for the planning, execution, issue resolution, and communication / communication planning required for successful execution of each assigned ...

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$22.8K

$55.5K

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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.

Study Team Associate (Per Diem)

Thermo Fisher Scientific

Austin, TX • On-site

Part-time

Re-posted 11 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

197th of 536 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Shift Detail: Per Diem (as needed/no guaranteed hours); flexibility to cover all shifts as clinic operates 24/7; average availability requested ~29hrs/week
Keys to Success:
Location/Division Specific Information
Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we collaborate with clients to define and develop clinical programs, reduce delays, and implement high-quality, cost-efficient clinical studies.
Discover Impactful Work:
Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for supporting all study management roles within Clinical Operations. This entails tasks within the screening, study conduct and data entry phases of the trials. Inclusive of, but is not limited to, conducting a screening session to provide the Informed Consent session as delegated by the Principal Investigator, coordinating and performing tasks associated with checking in, checking out and conducting outpatient visits for participants actively enrolled in studies as well as performing a variety of team related procedures. Supports team members within their own study team as well as other study teams within the Clinical Operations department.
A day in the Life:
  • Fulfills all training expectations associated with tasks that support clinical trials within the study management roles

  • Serves as back up, when needed, for study primaries within the Enrollment, Coordinating and Data Entry positions.

  • Completes administrative tasks such as preparing, reviewing and verify source as well as coordinating management of supplies for upcoming visits.

Education
  • High school diploma or equivalent required.

Experience
  • Previous applicable experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).

  • In some cases, a combination of appropriate education, training and/or directly related experience will be considered sufficient and equivalent for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities
  • Demonstrated ability handling multiple responsibilities and completion of projects with overlapping prioritization.

  • Basic computer skills including knowledge of Microsoft Office and the ability to learn various programs and/or data management or electronic source systems.

  • Strong communication skills. Ability to clearly explain information to a wide variety of individuals.

  • Ability to work closely with multiple types of individuals in potentially difficult or uncomfortable settings.

  • Strong attention to detail with strong planning and organization capabilities to manage multiple tasks and multiple study groups at one time.

  • Effective time-management while demonstrating ability to communicate need for assistance.

Physical Requirements / Work Environment
  • Work is performed in an office or clinical environment.

  • Frequent long hours, weekends, and/or holidays.

  • Exposure to blood and biohazardous waste.

  • Be available by cell phone after hours.

  • Potential occasional travel required.

Physical Requirements:
  • Frequently vertical and /or stationary for 6-8 hours per day.

  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.

  • Frequent mobility required.

  • Frequent bending and twisting of upper body and neck.

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

  • Ability to communicate moderately complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

  • Frequently interacts with others, relates sensitive information to diverse groups.

  • Ability to apply basic principles to solve conceptual issues.

  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence.

  • Ability to perform under stress.

  • Ability to multi-task.

  • Regular and consistent attendance.

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