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Esource Jobs in Texas (NOW HIRING)

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Lab Analyst I (MLT/MT- ASCP)

San Antonio, TX · On-site

Utilizes the Laboratory Information System and eSource system. * Provides notification and documentation of critical laboratory values obtained to Principal Investigator. * Participates in the ...

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Lab Analyst I (MLT/MT- ASCP)

Houston, TX · On-site

Utilizes the Laboratory Information System and eSource system. * Provides notification and documentation of critical laboratory values obtained to Principal Investigator. * Participates in the ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$40K - $48K/yr

Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.

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How much do esource jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for esource in Texas is $23.17, according to ZipRecruiter salary data. Most workers in this role earn between $13.32 and $27.06 per hour, depending on experience, location, and employer.

What are the main responsibilities of an Esource Specialist in a clinical research setting?

As an Esource Specialist, your primary responsibilities include implementing and maintaining electronic source data systems for clinical studies, ensuring data accuracy, and supporting compliance with regulatory standards. You will often work closely with clinical research coordinators, data managers, and IT teams to set up, test, and troubleshoot eSource platforms. Additionally, you may assist in training site staff, creating documentation, and participating in data quality audits. This role is a key part of the clinical research process, helping streamline workflows and contribute to the reliability of study outcomes.

What is an Esource job?

An Esource job typically involves managing electronic source data in clinical research or healthcare settings. Professionals in this role ensure the accurate collection, storage, and integration of digital records, often replacing traditional paper documentation. They may work with electronic data capture (EDC) systems, regulatory compliance, and data quality control. Strong attention to detail and familiarity with clinical or regulatory environments are essential.

What are the key skills and qualifications needed to thrive in the Esource position, and why are they important?

To succeed as an Esource Specialist, you need a background in clinical research, an understanding of data management, and familiarity with regulatory guidelines, often supported by a degree in life sciences or a related field. Expertise in electronic data capture (EDC) systems, eSource platforms such as Medidata Rave or OpenClinica, and possibly certifications in clinical data management are highly valued. Attention to detail, problem-solving ability, and strong collaboration skills are essential for working with research teams and ensuring data integrity. These competencies are vital to ensure accurate, compliant, and efficient collection and management of clinical trial data.

What are popular job titles related to Esource jobs in Texas? For Esource jobs in Texas, the most frequently searched job titles are:
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Esource jobs near you
Infographic showing various Esource job openings in Texas as of June 2026, with employment types broken down into 77% Full Time, and 23% Part Time. Highlights an 100% In-person job distribution, with an average salary of $48,185 per year, or $23.2 per hour.
Site System Associate II

Site System Associate II

DM Clinical Research

Houston, TX • On-site

Full-time

Posted 9 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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