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Medtronic
Medtronic
H1B vizos rėmėjasGamybaSveikatos draudimasSveikatos priežiūra
„Medtronic“ yra pasaulinė sveikatos priežiūros technologijų ir gamybos įmonė, kurianti sprendimus sudėtingoms medicininėms būklėms gydyti. Jos veikla apima dideles tarptautines komandas ir glaudų bendradarbiavimą su sveikatos priežiūros specialistais, siekiant gerinti gydymą, terapijas ir medicinos technologijų prieinamumą. Daugiau nei 95 000 darbuotojų daugiau kaip 150 šalių turinti „Medtronic“ daugiausia dėmesio skiria pacientų priežiūros pažangai, taip pat puoselėja įtrauktį, įvairovę, lygybę ir tvarią veiklą visose savo operacijose.
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Darbai įmonėje

Clinical Research Specialist, Neurovascular Studies

Oversee clinical study sites, data quality, and regulatory records for Medtronic’s neurovascular technologies. Support compliant studies from site activation through closeout.

USJungtinės ValstijosCAKalifornijaCOKoloradasMNMinesota
83 200 $ – 124 800 $ / metai
Darbas vietojeVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Oversee clinical study sites from activation to closeout, handling initiation, training, issue resolution, and ongoing support.
  • Review and maintain regulatory and study-startup records, including approvals.
  • Coordinate investigators and site staff to uphold protocols, data quality, and study goals.
  • Maintain study files, essential records, training materials, and other documentation.
  • Review 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 documents.
  • Track study progress and report on clinical investigation activities, milestones, and results.
  • Work with study sites, vendors, and cross-functional teams to support study delivery.

Reikalavimai

  • Clinical 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 in clinical research, clinical operations, or related study support.
  • Experience supporting clinical studies and managing clinical site activities.
  • 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 degrees earned outside the United States, a baccalaureate degree meeting 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Privalumai

  • Competitive pay 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 contributions and matching.
  • Short-term disability.
  • Paid time off.
  • Paid holidays.
  • Employee Stock Purchase Plan.
  • Employee Assistance Program.
  • Supplemental non-qualified retirement plan.
  • Capital Accumulation Plan for vice presidents and above, or employees meeting IRS earnings thresholds.
  • Temporary employees receive paid sick time as required by applicable state law.
  • Employee Stock Purchase Plan for temporary employees.

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