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Medtronic

Clinical Research Program Manager – MCRS Strategic Account Manager

Medtronic

Clinical 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 fit
Core 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

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Applicant 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 & technologies
PMP

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