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Esource Jobs (NOW HIRING)

Clinical Ink

eSource Developer III

The eSource Developer III will serve as a subject matter expert and design and build electronic source documents that align with protocol requirements, ensuring quality, consistency, and usability.

Crio, Inc.

Sr. Director of Sponsor Operations

$160K - $185K/yr

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

ESource Corp

Fractional Learning Leader

Sparta, NJ · On-site

Company Description ESource is a leader in training and development, staffing, and consulting services since 1995. We have a global network of L&D consultants, trainers, and instructional designers ...

ESource Corp

Fractional Learning Leader

Sparta, NJ · On-site +1

Company Description ESource is a leader in training and development, staffing, and consulting services since 1995. We have a global network of L&D consultants, trainers, and instructional designers ...

Jj

Senior Data Acquisition Expert

Horsham, PA · On-site +1

Data Acquisition Expert eSource role-specific responsibilities: * Accountable for the setup & maintenance of eSource within assigned trial(s)/program according to best practices and defined ...

Crio, Inc.

Director of Sponsor Operations

$150K - $170K/yr

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

Jj

Senior Data Acquisition Expert

Titusville, NJ · On-site +1

Data Acquisition Expert eSource role-specific responsibilities: * Accountable for the setup & maintenance of eSource within assigned trial(s)/program according to best practices and defined ...

Jj

Senior Data Acquisition Expert

Raritan, NJ · On-site +1

Data Acquisition Expert eSource role-specific responsibilities: * Accountable for the setup & maintenance of eSource within assigned trial(s)/program according to best practices and defined ...

Jj

Senior Data Acquisition Expert

Spring House, PA · On-site +1

Data Acquisition Expert eSource role-specific responsibilities: * Accountable for the setup & maintenance of eSource within assigned trial(s)/program according to best practices and defined ...

Johnson County Clin Trials

Quality Specialist

$30/hr

Review draft source document templates paper records and eSource (CRIO) for accuracy, completeness, and compliance with study protocols, CRF completion guidelines, SOPs and sponsor requirements

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Esource information

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.

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Esource jobs near you
Infographic showing various Esource job openings in the United States as of July 2026, with employment types broken down into 1% Internship, 86% Full Time, 6% Part Time, and 7% Contract. Highlights an 70% Physical, and 30% Remote job distribution.
eSource Developer III

eSource Developer III

Clinical Ink

Remote

Full-time

Posted 16 days ago

Job description

Company Information
Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.
Job Description
Clinical Ink is seeking an eSource Developer III to join our Study Operations team based remotely across the United States. The eSource Developer III will serve as a subject matter expert and design and build electronic source documents that align with protocol requirements, ensuring quality, consistency, and usability. This role partners with cross-functional stakeholders, mentors other team members, and drives efficient, standards-based workflows in a fast-paced, quality controlled environment. The eSource Developer III's responsibilities include:
  • Program and review logic throughout the build process to confirm that specifications and requirements are suitable for users’ needs
  • Create, modify, and maintain electronic source documents based on protocol specifications or provided requirements
  • Review, recommend, implement, and utilize coding standards to maintain consistent workflow across team
  • Reference protocol and/or other documentation to ensure expectations are met
  • Train and mentor new eSource Development team members including tracking training progress, training new team members on product functionality, use, and design, and shadowing new team member on new study builds
  • Apply version control specifications to maintain document integrity and historical data
  • Communicate with other teams to ensure consistency within and across studies
  • Maintain client requests and updates in fast paced, quality-checked environment
  • Create printable paper source forms for user convenience, as needed
  • Provide technical assistance with problem solving for tickets
  • Work with Project Management and Study Build in drafting, reviewing, approving, and updating applicable project build and change control timelines
  • Other duties as assigned
Qualifications
  • Bachelor’s degree in Computer Science or equivalent work experience
  • At least five years in a full-time programming role
  • Strong programming skills (JavaScript/C#) and ability to code required
  • Ability to conceptualize large study builds and anticipate programming/coding challenges
  • Ability to organize, instruct and supervise staff, while promoting group effort in a matrix environment
  • Working knowledge of one or more Agile methodologies (i.e. TDD, SCRUM, or R-SCRUM)
  • Ability to identify needs and issues, track progress, and follow through on actions to meet customer satisfaction
  • Ability to communicate needs, issues, impacts, and corrective actions to varying levels of corporate personnel and customer leadership personnel
  • Demonstrated ability to manage conflicts and resolve problems effectively
  • Excellent written, verbal, and interpersonal communication skills; organizational skills and great attention to detail are required
  • Knowledge of complex scientific/office procedures and techniques relating to clinical research and patient care to accurately design source documents used to conduct clinical trials, preferred
Additional Information
Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
www.clinicalink.com ​

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