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Research Project Manager
ŌURA. 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 .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing human research and clinical studies, with a focus on project management, documentation, and risk management. Proficient in building strategic partnerships and ensuring compliance with privacy and consent requirements.
Highest-signal resume keywords
Human Research ManagementProject ManagementRisk ManagementCross-Functional CommunicationGCP/CITI Training
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchHealth OutcomesReal-World EvidenceStudy PlanningData CollectionReportingDocumentationBudget CoordinationIssue ResolutionData Quality Review
Soft Skills
Relationship BuildingStakeholder CommunicationProblem Solving
Tools & Technologies
SpreadsheetsProject TrackersSurvey PlatformsEHRsEDCCTMSETMF
Certifications & Qualifications
GCP TrainingCITI Training
Industry Keywords
Healthcare ProgramsCRO PartnershipsAcademic CollaborationsCommercial ResearchParticipant Privacy
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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 relationships with strategic collaborators in academic, healthcare, CRO, and commercial organizations
- Establish repeatable processes, workflows, and documentation for high-quality research at industry speed and scale
- Translate research questions into study plans, operational requirements, documented decisions, milestones, reporting, and evidence deliverables with expert teams
- 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 to internal and external stakeholders
- Support evidence dissemination through reports, publications, abstracts, partner deliverables, clinical education, and commercial or regulatory materials
Requirements
What you’ll need- 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
Benefits
Comp & perks- Oura provides what team members need to do their best work both in and out of the office
- Hybrid or office settings available for employees who prefer them
- Reasonable accommodation to participate in the interview process, perform essential job functions, and receive other benefits and privileges of employment