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Eclinical Jobs (NOW HIRING)

Coordinate overall eClinical activities by serving as primary contact for the sponsor; * Monitor study timelines in relation to clinical trial needs; * Attend face to face sponsor meetings and ...

Senior Software Engineer

$125K - $165K/yr

Job Summary : eClinical Solutions is transforming clinical development with elluminate ® , their Clinical Data Cloud that helps life sciences organizations unify, analyze, and unlock the value of ...

Senior Software Engineer

$125K - $165K/yr

Job Summary : eClinical Solutions is transforming clinical development with their Clinical Data Cloud, elluminate ® . They are seeking a Senior Software Engineer to design and develop core modules ...

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the value ...

Senior Software Engineer

Mansfield, MA · On-site +1

$129K - $171K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

Senior Software Engineer

Mansfield, MA

$129K - $171K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the value ...

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the value ...

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Eclinical information

See salary details

$42K

$86.6K

$128K

How much do eclinical jobs pay per year?

As of Aug 27, 2026, the average yearly pay for eclinical in the United States is $86,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,500.00 and $108,000.00 per year, depending on experience, location, and employer.

What is eclinical?

eClinical refers to the use of electronic systems and software to support the planning, management, and conduct of clinical trials. Professionals in eClinical work with technologies such as electronic data capture (EDC), clinical trial management systems (CTMS), and electronic patient-reported outcomes (ePRO) to streamline data collection, improve trial efficiency, and ensure regulatory compliance. Their tasks often include implementing digital tools, training clinical staff, managing data integrity, and ensuring that all electronic processes adhere to industry standards and regulations.

What are the key skills and qualifications needed to thrive as an eclinical specialist?

To thrive as an Eclinical Specialist, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with EDC systems (such as Medidata Rave or Oracle InForm), CTMS platforms, and GCP certification is typically required. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration with study teams. These skills are crucial for maintaining high-quality clinical trial data and supporting successful study outcomes in a regulated environment.

What are some common challenges faced by professionals working in eclinical roles, and how can they be addressed?

EClinical professionals often encounter challenges such as adapting to rapidly evolving technology, ensuring data integrity across multiple systems, and maintaining compliance with regulatory requirements. Staying updated with software platforms and industry best practices is crucial, as is effective collaboration with clinical, data management, and IT teams. Building strong communication skills and participating in ongoing training can help address these challenges and contribute to successful clinical trial outcomes.

What is the difference between Eclinical vs Clinical Data Coordinator?

AspectEclinicalClinical Data Coordinator
Required CertificationsExperience with EDC systems, possibly certifications in clinical data managementLikely similar certifications, including data management and clinical research training
Work EnvironmentTypically works with electronic data capture (EDC) systems in clinical trialsManages and verifies clinical trial data, often using EDC systems
Employer & Industry UsageUsed by clinical research organizations, pharmaceutical companies, CROsCommonly employed in clinical research settings, hospitals, and biotech firms

Both roles involve handling clinical trial data, with Eclinical focusing on electronic systems and data management platforms, while Clinical Data Coordinators primarily verify and manage trial data. They often work together within the same industry environment, making their skills and certifications closely aligned.

More about Eclinical jobs

What cities are hiring for Eclinical jobs?

Cities with the most Eclinical job openings:

What are the most commonly searched types of Eclinical jobs?

The most popular types of Eclinical jobs are:

What states have the most Eclinical jobs?

States with the most job openings for Eclinical jobs include:

Infographic showing various Eclinical job openings in the United States as of August 2026, with employment types broken down into 2% Locum Tenens, 1% As Needed, 88% Full Time, 7% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $86,556 per year, or $41.6 per hour.

eClinical Project Manager

Cincinnati, OH • On-site, Remote


Medpace, Inc.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Great coworkers

People enjoy working here

Good employer


Full-time

Medical, Retirement, PTO

Re-posted 26 days ago


Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based eClinical Project Manager to join our Data Management team in our Cincinnati, OH office. This role will work with both local and international teams and will manage global studies. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Manage multiple projects from am eClinincal/eCOA perspective;
  • Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments; 
  • Coordinate overall eClinical activities by serving as primary contact for the sponsor;
  • Monitor study timelines in relation to clinical trial needs;
  • Attend face to face sponsor meetings and Investigator Meetings
Qualifications
  • Bachelor's degree and prior eClinical experience; including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor;
  • General knowledge of technology trends and system / application development;
  • Possess excellent organizational, prioritization, and time management skills;
  • A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992


What Medpace employees say

Pay

Benefits

Hours and flexibility

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