via Glassdoor
$79K - 118K a year
Manage a portfolio of decentralized clinical trials, leading cross-functional teams to ensure study success and compliance.
Bachelor's degree in a biological or health-related field, at least 2 years in clinical research or project management, with strong communication and organizational skills.
This a Full Remote job, the offer is available from: United States Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career! EmVenio provides quality, in-home clinical trial visits for various Sponsors and CROs. We're the only company that hires, trains, certifies, tests, and manages our own Certified Mobile Research Nurses (CMRNs). Our mission is to bring clinical trial visits to subjects wherever they may be to increase convenience and compliance with study protocols. Be part of a team who fully embrace our values and key behaviors • We work as a team • We do the right thing • We figure it out • We pursue growth • We take ownership Why work for PCM TRIALS? • Contribute to advancements of truly life changing treatments • Provide alternative modalities to enhance diversity in clinical research subject pools • Liaise with industry innovators to promote decentralized approaches to clinical research Summary We are currently seeking an experienced Clinical Project Manager to manage a portfolio of decentralized clinical trials. In this position, you will lead multiple cross-functional teams to execute clinical research studies that evaluate whether new treatments, such as new drugs or medical devices, are safe and effective. Be part of this exciting team that is committed to helping others and moving science forward. This position is eligible to be performed as a remote position. Required Qualifications • Bachelor’s degree from an accredited four-year college or university in a biological program. • Two or more years of experience in the clinical research industry or equivalent. • Two or more years of experience in project management, for delivering assigned projects within time, scope, and cost. • Detail oriented, with excellent verbal, and written communication skills as the central liaison for clients and stakeholders within assigned projects. Preferred Qualifications • Clinical trial management and coordination • Risk mitigation and Issue Resolution – Proactively identifies and mitigates risks. Resolves and documents issues in real-time. • Contribute to the continuous improvement of all processes. • Lead by example and manage subordinates as a coach to help coordinators be successful. #LI-CMR1 #LI-REMOTE The typical base pay range for this role is USD $78,700 - $118,000 per year. Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors. Available Benefits Include • Medical • Dental • Vision • 401(k) • Company Paid Short Term Disability • Flexible Spending Account (FSA) • Health Savings Account (HSA) • Paid Time Off • Voluntary Benefits Please contact Carson Moreira-Rego at (866) 776-0127 x387 or at Carson.Moreira-Rego@procasemanagement.com today to learn more about our opportunities where you can make a difference in your own career! Professional Case Management is an Equal Opportunity Employer. This offer from "Professional Case Management" has been enriched by Jobgether.com and got a 76% flex score.
This job posting was last updated on 1/9/2026