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Medtronic
Medtronic
Sponsor pentru viza H1BAsigurare de sănătateAsistență medicalăIndustria prelucrătoare
Medtronic este o companie globală de tehnologie medicală și producție, care dezvoltă soluții pentru afecțiuni medicale complexe. Activitatea sa reunește echipe internaționale numeroase și o colaborare strânsă cu profesioniștii din domeniul sănătății pentru a îmbunătăți tratamentele, terapiile și accesul la tehnologia medicală. Cu peste 95.000 de angajați în mai mult de 150 de țări, Medtronic se concentrează pe dezvoltarea îngrijirii pacienților, susținând totodată incluziunea, diversitatea, echitatea și practicile sustenabile în cadrul operațiunilor sale.
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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.

USStatele Unite ale AmericiiCACaliforniaCOColoradoMNMinnesota
83.200 $ – 124.800 $ / an
La sediuNormă întreagăJuniorNivel mediuNu este necesară o diplomăLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • 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.

Cerințe

  • 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).

Beneficii

  • 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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