Job Description
Research Project Coordinator
Milwaukee, WI (Preferred; US-based candidates)
Hybrid Role (Onsite preferred; remote / hybrid flexibility after onboarding)
Duration : ASAP through June 30, 2026 (Extension possible)
ABOUT THE ROLE
- Medasource is seeking two Research Project Coordinators to support clinical and operational research within a leading global medical device and healthcare technology organization. Based in Milwaukee, WI, with remote or hybrid options available after initial training, these roles are responsible for driving study execution, maintaining high-quality documentation, and coordinating research operations across patient-monitoring, acute-care, and maternal–infant-care technology portfolios. You will support multiple ongoing clinical studies and evidence-generation initiatives, focusing on meeting coordination, study documentation, QMS support, site engagement, and overall research operations. This is an excellent opportunity for experienced research coordinators or project specialists looking to advance their impact in a regulated med-tech environment, with flexibility for hybrid or remote work following successful onboarding.
WHAT YOU'LL DO
Participate in recurring study meetings; capture detailed minutes, decisions, and action itemsTrack follow-up activities and ensure timely closure with cross-functional teamsHelp maintain project timelines, trackers, dashboards, and study artifactsManage study documents, deliverables, trackers, and vendor invoicesSupport Quality Management System (QMS) documentation practices and version controlMaintain organized electronic study files and ensure audit-ready documentationEngage with research sites to support timelines, data requests, and study logisticsTrack study milestones, enrollment, and operational metricsCoordinate with internal partners across Clinical, Quality, Regulatory, and Product teamsAssist with protocol updates, controlled document management, and evidence-generation tasksSupport research operations and process initiatives across the team as neededWHAT YOU BRING
3+ years experience in clinical research, medical device research, med-tech, or regulated healthcare settingsWorking knowledge of Good Clinical Practice (GCP) and Quality Management System (QMS) documentation (ISO 13485 or similar)Strong skills in meeting facilitation, action tracking, and structured communicationExcellent written and verbal communication abilitiesProficiency in MS Teams, SharePoint / OneDrive, and Excel-based trackersAbility to work independently after onboardingExperience supporting multi-site clinical studies (preferred)Familiarity with protocol management, controlled documentation, or ClinicalTrials.gov submissions (preferred)Exposure to medical device research, post-market clinical follow-up, or evidence generation (preferred)Understanding of patient monitoring, maternal–infant care, or acute-care device environments (preferred)Preference for candidates based in the United States working standard US business hoursWHAT'S IN IT FOR YOU
Opportunity to advance your impact in a regulated med-tech environmentHybrid or remote work flexibility after successful onboardingCollaborative, cross-functional team environmentExposure to global medical device and healthcare technology researchPotential for contract extension beyond June 2026