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Study Management Associate Jobs in Texas (NOW HIRING)

DM Clinical

Study Manager I (3767)

Houston, TX · On-site

$80K - $96K/yr

Responsible for clinical trial management from FPFV to study close out with strict adherence to ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...

Daymon

Associate Business Manager, Own Brands

Tyler, TX · On-site

Summary Associate Business Manager At our Company, we grow People, Brands, and Businesses! We are ... Study/Area of Experience: Business 0-2 Years of experience in Account or Brand Management Skills ...

Daymon

Associate Business Manager, Own Brands

Tyler, TX · On-site

$50K - $63K/yr

Summary Associate Business Manager At our Company, we grow People, Brands, and Businesses! We are ... Study/Area of Experience: Business 0-2 Years of experience in Account or Brand Management Skills ...

Pwc

Data Engineer - Senior Associate

Dallas, TX

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

Pwc

Data Engineer - Senior Associate

Austin, TX · On-site

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

Pwc

Data Engineer - Senior Associate

Houston, TX · On-site

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

Pwc

Data Engineer - Senior Associate

San Antonio, TX

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

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How much do study management associate jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for study management associate in Texas is $35.49, according to ZipRecruiter salary data. Most workers in this role earn between $23.47 and $46.30 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are the typical responsibilities of a Study Management Associate in a clinical research team?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What is a Study Management Associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.
What are popular job titles related to Study Management Associate jobs in Texas? For Study Management Associate jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Study Management Associate jobs in Texas look for? The top searched job categories for Study Management Associate jobs in Texas are:
Study Management Associate jobs near you
Study Team Associate (Per Diem)

Study Team Associate (Per Diem)

Thermo Fisher Scientific

Austin, TX • On-site

Part-time

Posted 6 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 409 frontline employees who took The Breakroom Quiz

190th of 527 rated manufacturers

Job description

Work Schedule
Other
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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