3 дня назад
Clinical Research Lab RN (Medical Devices)
100 000 - 120 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Lab RN (Medical Devices): Executing and documenting clinical studies for medical device R&D, regulatory submissions, and marketing initiatives with an accent on patient procedures, data integrity, and clinical protocol compliance. Focus on conducting invasive clinical procedures, monitoring subjects and adverse events, and preparing study documentation in accordance with GCP and FDA requirements.
Location: Irvine, California, United States; on-site role with an eligible remote work arrangement also available
Salary: $100,000–$120,000 annually, plus eligibility for up to a 10% annual bonus
Company
operating company Masimo develops medical monitoring technologies, sensors, patient monitors, and automation and connectivity solutions.
What you will do
- Execute and document clinical studies supporting product research and development, regulatory filings, and marketing initiatives.
- Perform venous punctures, finger sticks, blood draws, venous line removal, arterial dressing, intravenous catheter placement, and related patient care.
- Qualify subjects, collect medical histories, monitor vital signs, support arterial line placement, and assist with emergency medical administration.
- Set up equipment, manage study materials, follow protocols and clinical work instructions, collect data, verify results, and transfer documentation.
- Prepare or review study plans, informed consents, IRB submissions, case report forms, and other study materials.
- Support safety reviews, protocol deviation assessments, device deficiency investigations, and adverse event reporting.
Requirements
- Licensed RN in the state of California
- Current ACLS certification
- Excellent written and verbal communication skills.
- Advanced judgment and decision-making ability in clinical study execution and oversight.
- Ability to perform the required clinical procedures and support clinical research operations.
Nice to have
- Experience in medical, pharmaceutical, or medical device research.
- Understanding of FDA Good Clinical Practice guidelines for medical device studies.
- Experience with post-market surveillance or regulatory affairs submissions for medical devices.
- Clinical or scientific background.
Culture & Benefits
- Work within a life sciences and medical technology organization focused on clinical impact.
- Eligible employees receive paid time off and medical, dental, and vision insurance.
- Eligible employees can participate in a 401(k) plan.
- Flexible remote work arrangements may be available for eligible roles.
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