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Ōura
Posted 13 days agoVerified live 2d ago

Research Project Manager

Brief overview

Remote
UndergradOr in progress
3+ yrsMinimum
11 H-1B approvalsDept. of Labor
2 green cardsCertified filings
Human-subjects researchClinical researchReal-world evidenceResearch project managementResearch data flowsParticipant privacy and consentData-quality reviewClinical Practice (GCP)CITI trainingElectronic health records (EHRs)Electronic data capture (EDC)Clinical trial management systems (CTMS)Electronic trial master file (eTMF)Relationship managementRisk management

About the company

Global health technology company focused on wearable wellness devices.

Visa sponsorship history

4 years sponsoring, last filed FY2026

Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.
11H-1B approved
100%approval rate
1new H-1B hires
2PERM certified
$163,030median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
20233
20242
20253
20263
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20231
20242
20252
20264
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20231
20251
Top sponsored roles
Senior Director, Business SystemsSenior Machine Learning Data ScientistMCAD & PLM EngineerSenior Supplier Development EngineerSenior Algorithm Scientist
Sponsored employees from
China

Job description

Summary

ŌURA develops wearable technology and connected-app experiences that help people understand and improve their health, readiness, activity, and sleep. The Research Project Manager will manage strategic partnership research projects generating real-world evidence, coordinating internal teams and external collaborators from feasibility through closeout. The role will also establish research operations processes, manage project risks and logistics, and support evidence dissemination.

Responsibilities

  • Own a portfolio of commercial, academic, and member-based research studies, from feasibility and scoping through partner coordination, launch, data collection, analysis readiness, reporting, and closeout
  • Build and maintain strong relationships with strategic collaborators in academic, healthcare, CRO, and commercial organizations
  • Establish repeatable processes, workflows, and documentation to enable high-quality research at industry speed and scale in a highly dynamic environment
  • Work with teams of experts to translate research questions into clear study plans, operational requirements, documented decisions, milestones, reporting, and evidence deliverables
  • Coordinate budgets, contracts, partner responsibilities, data-transfer expectations, privacy and consent requirements, timelines, and issue resolution
  • Monitor study progress, surface risks early, and communicate tradeoffs clearly to internal and external stakeholders
  • Support evidence dissemination through reports, publications, abstracts, partner deliverables, clinical education, or commercial and regulatory materials as appropriate

Skills

  • 3+ years of experience managing human research, clinical research, health outcomes, real-world evidence, healthcare programs, or equivalent partner research programs
  • Experience independently managing external academic, commercial, clinical, CRO, and/or healthcare partnerships
  • Experience taking research or outcomes projects from feasibility and planning through execution, reporting, and closeout
  • Strong project-management, documentation, risk-management, and cross-functional communication skills
  • Familiarity with research data flows, participant privacy and consent, data-quality review, and tools such as spreadsheets, project trackers, survey platforms, EHRs, EDC, CTMS, eTMF, or comparable systems
  • Human-subjects research and GCP/CITI training, or willingness to complete required training
  • This is a remote US role
  • A slight preference for candidates based on the East Coast

Qualifications

Must Haves

  • 3+ years of experience managing human research, clinical research, health outcomes, real-world evidence, healthcare programs, or equivalent partner research programs
  • Experience independently managing external academic, commercial, clinical, CRO, and/or healthcare partnerships
  • Experience taking research or outcomes projects from feasibility and planning through execution, reporting, and closeout
  • Strong project-management, documentation, risk-management, and cross-functional communication skills
  • Familiarity with research data flows, participant privacy and consent, data-quality review, and tools such as spreadsheets, project trackers, survey platforms, EHRs, EDC, CTMS, eTMF, or comparable systems
  • Human-subjects research and GCP/CITI training, or willingness to complete required training
  • This is a remote US role

Nice to Haves

  • a slight preference for candidates based on the East Coast

Benefits

  • Remote US role
  • Hybrid or office settings available in San Francisco, San Diego, and Los Angeles

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