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Home Based Eclinical Jobs (NOW HIRING)

Coordinate overall eClinical activities by serving as primary contact for the sponsor; * Monitor ... Office based culture with occasional WFH that provides flexibility for eligible positions after ...

Coordinate overall eClinical activities by serving as primary contact for the sponsor; * Monitor ... Office based culture with occasional WFH that provides flexibility for eligible positions after ...

Patient Navigators provides all home-based HIV health promotion, support, and skills-building ... Experience with eSHARE and/or eClinical Works is preferred The following additional competencies ...

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This role is essential in helping eligible patients enroll in health home and community-based ... MAPP), eClinical Works (eCW), PSYCKES, Foothold Care Management (FCM). * Ability to travel ...

Clinic Phlebotomist

Cullman, AL · On-site

$14.75 - $18.50/hr

Vision insurance Are you an experienced phlebotomist looking for a new home? Cullman Internal ... based on state health laws and the guidelines of our medical organization · Answer patient ...

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Home Based Eclinical information

What is the difference between Home Based Eclinical vs Home Based Clinical Research Coordinator?

AspectHome Based EclinicalHome Based Clinical Research Coordinator
CertificationsOften requires EDC or clinical trial software training, basic clinical research knowledgeRequires GCP training, clinical research certification, and site-specific credentials
Work EnvironmentPrimarily remote, using electronic data capture and communication toolsRemote with some site visits or patient interactions, depending on study needs
Employer & IndustryPharmaceutical companies, CROs, biotech firms conducting remote data managementResearch sites, hospitals, or CROs managing patient recruitment and data collection

Home Based Eclinical roles focus on remote data management and electronic trial activities, while Home Based Clinical Research Coordinators handle patient interactions and site management, often requiring more direct clinical oversight. Both roles are essential in clinical trials but differ in responsibilities and work environment.

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Infographic showing various Home Based Eclinical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 13% Part Time, and 7% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution.

eClinical Project Manager

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 27 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research


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

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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