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Medtronic
Medtronic
H1B Visa SponsorHealthcareHealthcare InsuranceManufacturing
Medtronic is a global healthcare technology and manufacturing company developing solutions for complex medical conditions. Its work brings together large, international teams and close collaboration with healthcare professionals to improve treatments, therapies, and access to medical technology. With more than 95,000 employees across over 150 countries, Medtronic focuses on advancing patient care while supporting inclusion, diversity, equity, and sustainable practices across its operations.
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Clinical Research Specialist, Neurovascular Studies

Oversee clinical sites, study documentation, and data quality for Medtronic neurovascular device studies. Coordinate compliant study delivery with investigators, vendors, monitors, and internal teams.

USUnited StatesCACaliforniaCOColoradoMNMinnesota
$83,200 – $124,800 / year
On-siteFull-timeJuniorMiddleNo degree requiredEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Guide clinical study sites from activation to closeout, providing initiation, training, issue resolution, and ongoing support.
  • Review, approve, and maintain regulatory and study startup records.
  • Coordinate investigators and site staff to support protocol compliance, reliable data, and study goals.
  • Maintain study files, essential records, training materials, and other documentation.
  • Assess clinical data, resolve discrepancies, track outstanding queries, and coordinate study actions with monitors.
  • Help develop and carry out clinical management plans, protocols, case report forms, and related study materials.
  • Track study progress and report on investigation activities, milestones, and outcomes.
  • Work with sites, vendors, and internal teams to support effective study delivery.

Requirements

  • Clinical research, clinical operations, or related study support experience: 6+ years with a high school diploma or equivalent; 4+ years with an associate degree; 2+ years with a bachelor's degree; or an advanced degree.
  • Experience supporting clinical studies and managing clinical sites.
  • Experience working in accordance with Good Clinical Practice (GCP).
  • Experience reviewing clinical data, resolving discrepancies, and maintaining study records.
  • Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is unavailable for roles below Principal level.
  • For bachelor's degrees earned outside the United States, the degree must meet the standard in 8 C.F.R. § 214.2(h)(4)(iii)(A).

Benefits

  • Competitive salary and flexible benefits package.
  • Health, dental, and vision insurance.
  • Health Savings Account.
  • Healthcare Flexible Spending Account.
  • Life insurance.
  • Long-term disability leave.
  • Dependent care spending account.
  • Tuition assistance or reimbursement.
  • Simple Steps global well-being program.
  • Incentive plans.
  • 401(k) plan with employer contribution and match.
  • Short-term disability.
  • Paid time off.
  • Paid holidays.
  • Employee Stock Purchase Plan.
  • Employee Assistance Program.
  • Nonqualified Retirement Plan Supplement.
  • Capital Accumulation Plan for Vice Presidents and above, or employees meeting IRS earnings thresholds.

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