Field Clinical Specialist – IVL Cardiovascular Devices

Johnson Johnson

Springfield (MO)

Presencial

USD 90 000 - 130 000

Tempo integral

14 dias+

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Resumo da oferta

Johnson & Johnson is hiring a Field Clinical Specialist for Shockwave Medical Inc. in Columbia, MO. This field role provides case support to physicians during peripheral and coronary procedures using IVL technology.

You will train clinicians, present study materials, manage investigators, and coordinate data collection for clinical programs, with travel greater than 50% and cross‑functional collaboration.

Qualificações

  • Bachelor's degree or equivalent experience required.
  • 2+ years supporting interventional or surgical procedures, or 1 year industry life sciences/sales support.
  • Knowledge of GCP and regulatory guidelines for trials.
  • Demonstrated collaboration with regulatory agencies during studies.
  • Strong product knowledge and attention to detail.
  • Proficient with MS Office and data collection tools.

Responsabilidades

  • Provide physician and hospital staff training and case coverage.
  • Meet internal and external stakeholders' needs with urgency.
  • Present clinical study materials to support safe device use.
  • Manage study investigators and relationships with medical advisors.
  • Coordinate site retraining and data collection for database locks.
  • Handle territory travel and budget administration.
  • Perform other duties as assigned.

Conhecimentos

Clinical training
Interventional procedures
Regulatory compliance
Collaboration
Negotiation
Detail orientation
Travel readiness

Formação académica

Bachelor's degree in business, science, nursing or related fields

Ferramentas

MS Office
Word processing
Spreadsheets
Data collection

Descrição da oferta de emprego

Johnson & Johnson is hiring a Field Clinical Specialist for Shockwave Medical Inc. in Columbia, MO. This field role provides case support to physicians during peripheral and coronary procedures using IVL technology.

You will train clinicians, present study materials, manage investigators, and coordinate data collection for clinical programs, with travel greater than 50% and cross‑functional collaboration.

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