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Clinical Project Associate Jobs in Texas (NOW HIRING)

Chenega Reliable Services

... project staff. * Responsible for patient evaluations, communications to pharmaceutical sponsors ... Associate degree in Nursing (ADN) * Possess and maintain an active and unencumbered Registered ...

C2 Alaska, LLC

Clinical Research Nurse

San Antonio, TX · On-site

... project staff. * Responsible for patient evaluations, communications to pharmaceutical sponsors ... Associate degree in Nursing (ADN) * Possess and maintain an active and unencumbered Registered ...

Chenega Reliable Services

... project staff. * Responsible for patient evaluations, communications to pharmaceutical sponsors ... Associate degree in Nursing (ADN) * Possess and maintain an active and unencumbered Registered ...

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Clinical Project Associate information

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$11

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$51

How much do clinical project associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical project associate in Texas is $29.38, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $38.75 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Texas? The most popular types of Clinical Project jobs in Texas are:
What are popular job titles related to Clinical Project Associate jobs in Texas? For Clinical Project Associate jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Project Associate jobs in Texas look for? The top searched job categories for Clinical Project Associate jobs in Texas are:
What cities in Texas are hiring for Clinical Project Associate jobs? Cities in Texas with the most Clinical Project Associate job openings:
Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Texas as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $61,120 per year, or $29.4 per hour.

Site System Associate II

DM Clinical Research

Houston, TX

Full-time

Re-posted 3 days ago

Job description

Site System Associate II
The purpose of this position is to provide technical expertise and organize the support of the Site Systems such as eSource, eConsent, eRegulatory, Looker, etc..to all DM Clinical Research Sites. The incumbent will serve as the first point of contact for matters related to site systems. The incumbent will have to work closely with all branches of Central Services as well as other functional teams across DM Clinical Research. The incumbent may be involved in identifying and researching new tools/systems that may be useful for DM Clinical Research. The incumbent may also provide support during deployment based on Site System Manager guidance.
DUTIES amp; RESPONSIBILITIES
  • Perform the development of each study into the electronic source, setting up new users and giving them access to the system based on set internal policies.
  • Perform finance configuration-related tasks based on departmental needs.
  • Act as the primary point of contact for any site system-related queries and questions
  • Contribute to the configuration, migration, User Acceptance Testing (UAT), validation, implementation, and maintenance of the eSource, eConsent, eRegulatory, Payment system, transportation system, looker, and any systems that come under Site Systems.
  • Collaborate with Clinical Operations Leadership on Super-User strategy to broaden end-user support and training.
  • Responsible for any special projects and tasks assigned by the manager or senior leadership.
  • Provide relevant audit support during inspections.
  • Identify opportunities for continuous process improvement; recommend solutions and implement them as needed
  • Any other matters as assigned by management

KNOWLEDGE amp; EXPERIENCE
Education:
  • BA/BS degree required
Experience:
  • 6 month working experience required in site system OR candidate must have 2 year of Clinical Research work experience
Credentials:
  • N/A
Knowledge and Skills:
  • Knowledge of any following vendor system: eSource Design, transportation portal, eConsent portal
  • Ability to manage User management of vendor system on own
  • Ability to multitask, communicate with internal stakeholders and gather system requirements
  • Knowledge of general system workflows, GCP guidelines, ALCOA-C related to electronic systems in clinical research.

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