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Clinical Research Program Manager – MCRS Strategic Account Manager
MedtronicClinical Research Program Manager advancing Medtronic’s global clinical evidence generation and regulatory approvals. Managing strategic healthcare partnerships, portfolios, business development, and risk.
Posted 9/10/2026full-timeRemote • Minnesota • 🇺🇸 United StatesMid-LevelSenior💰 $132,800 - $199,200 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research, regulatory strategies, and stakeholder management, with a strong focus on business development and performance management within the healthcare and medical device sectors.
Highest-signal resume keywords
Clinical Research ManagementRegulatory Affairs ExpertiseStrategic Account ManagementBusiness DevelopmentPortfolio Management
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 TrialsData AnalysisBudget ManagementProposal DevelopmentMarket IntelligenceQuality SystemsCompliance ProcessesPerformance ReviewsRisk ManagementEvidence Generation
Soft Skills
Relationship BuildingLeadershipCommunicationCollaborationNegotiation
Certifications & Qualifications
PMPAdvanced Degree (MBA, Master's)
Industry Keywords
HealthcareMedical DevicePharmaceuticalCROLife Sciences
Tech Stack
Tools & technologiesPMP
About the role
Key responsibilities & impact- Serve as the primary contact for Operating Unit/regional leaders and MCRS stakeholders
- Build and manage strategic stakeholder relationships and internal collaboration
- Identify opportunities for clinical evidence generation and new business
- Facilitate strategic discussions and communicate service capabilities and offerings
- Generate leads through networking and outreach
- Manage service offerings, track progress, and analyze customer needs
- Oversee proposal and negotiation processes, including potential outsourcing
- Develop and execute strategic plans using data analysis, benchmarking, and market intelligence
- Oversee portfolio-level deliverables, timelines, budgets, performance, quality, and financial status
- Conduct service delivery performance reviews and drive continuous improvement
- Manage portfolio-level risks and issues in collaboration with Quality and Compliance teams
- Lead end-to-end issue resolution and ensure escalation and resolution of quality, safety, timeline, and budget issues
- Provide leadership for clinical studies and regulatory affairs supporting product approval
- Develop and implement regulatory strategies for timely worldwide product approvals
- Ensure regulatory submissions are accurate and compliant
- Represent Medtronic in clinical research matters within the country/region and collect feedback from customers and authorities
- Lead local and global studies and manage clinical research projects across Medtronic therapies and businesses
Requirements
What you’ll need- Bachelor's degree
- 5+ years of related clinical experience (3+ years with an advanced degree)
- Experience in clinical research, clinical operations, strategic account management, business development, or portfolio management within healthcare, medical device, pharmaceutical, CRO, or related life sciences organizations
- Experience building and influencing relationships across complex, global matrix organizations and leading strategic customer or business partner engagements
- Knowledge of clinical trials, evidence generation, regulatory requirements, quality systems, and compliance processes
- Experience managing business performance, including budgets, forecasting, proposals, contracts, vendor oversight, and portfolio-level planning
- Advanced degree (MBA, Master's) or relevant certification (PMP), and experience developing business cases, growth strategies, or market assessments
- For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
- Candidates for roles below the Principal level must possess unrestricted U.S. work authorization at the time of hire and for the duration of employment
Benefits
Comp & perks- Competitive salary and flexible Benefits Package
- Short-term incentive through the Medtronic Incentive Plan (MIP)
- Health, Dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps (global well-being program)
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement
- Capital Accumulation Plan