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Emerald Clinical

Clinical Project Manager – Renal

Emerald Clinical

Experienced Project Manager in Clinical Operations for Emerald Clinical Trials managing global and regional clinical trials. Focused on Renal clinical trials with a commitment to quality and scientific excellence.

Posted 5/22/2026full-timeRemote • 🇧🇪 BelgiumSeniorLeadWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide strong, independent leadership for assigned clinical projects, ensuring successful execution.
  • Serve as the primary point of contact for clients, vendors, and internal stakeholders.
  • Oversee study management activities, including site selection, initiation, monitoring, and closeout.
  • Develop and maintain study timelines, budgets, and project plans, ensuring adherence to scope.
  • Mitigate risks and proactively address challenges to keep projects on track.
  • Ensure compliance with ICH-GCP, regulatory guidelines, and company SOPs.
  • Manage vendor relationships and study-specific contracts.
  • Provide mentorship and guidance to junior project team members.
  • Support proposal development, bid defense meetings, and business growth initiatives.
  • Participate in internal and external project team meetings to ensure alignment and success.

Requirements

What you’ll need
  • Bachelor’s or Masters degree in a science or related field
  • Previous experience working on clinical projects within an academic, CRO or pharmaceutical company environment
  • Experience in Renal is mandatory
  • Relevant work experience recommended for this role includes approximately seven (7) years of industry experience. A minimum of two (2) years of Project Management experience within the CRO industry is mandatory.
  • Prior experience as a CRA, in site management, trial coordination, or other relevant industry experience is preferred.
  • Experience managing single or different regions, working across different therapeutic indications, managing full-service studies, worked across early phase to Late phases of clinical trial, is preference
  • Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions.
  • Previous exposure to client-facing interactions and/or client management
  • Project finance management experience, CRO preferred.

Benefits

Comp & perks
  • Competitive Compensation : A tailored salary and benefits package to reflect your skills and experience.
  • Flexibility : Enjoy hybrid or remote working arrangements, depending on your location and role.
  • Career Growth : Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
  • Employee Wellbeing : Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
  • Global Opportunities : Be part of a company with international reach, offering you exposure to diverse projects and clients.

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
project managementclinical project executionstudy managementsite selectionmonitoringbudget managementrisk mitigationICH-GCP compliancevendor managementproposal development
Soft Skills
leadershipcommunicationmentorshipproblem-solvingcollaborationclient managementorganizational skillsadaptabilityteam alignmentguidance