5 часов назад
Solution Support Device SME
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Solution Support Device SME (Clinical Trial Medical Devices): Providing technical support for medical devices and associated applications at clinical trial sites, with an accent on device connectivity, data acquisition, and transmission. Focus on independently resolving complex support cases, performing root-cause analysis, maintaining troubleshooting documentation, and coordinating 24/7 support with US and European teams.
Location: Dalian, Liaoning, China; onsite
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Manage daily support activities and independently resolve complex cases submitted by clinical trial sites.
- Provide technical support for medical devices and associated applications.
- Diagnose and resolve issues involving device connectivity, data acquisition, and data transmission.
- Perform structured root-cause analysis to reduce repeat incidents and improve support quality.
- Create and maintain knowledge articles, how-to guides, and troubleshooting documentation.
- Collaborate with US and European teams to maintain a 24/7 global support model for APAC sites.
Requirements
- Bachelor’s degree in Life Sciences or a related field and at least 3 years of experience in an equivalent area.
- Foundational knowledge and practical experience in clinical trials, including familiarity with end-to-end trial and site operations.
- Familiarity with commonly used clinical trial medical devices; experience with deployment, configuration, calibration, or data acquisition validation is beneficial.
- Ability to work independently as the sole regional support member and proactively drive issue resolution.
- Fluent English in speaking, listening, reading, and writing, with strong cross-cultural communication skills.
- Ability to work across time zones in support of the global team.
Nice to have
- Clinical Research Associate (CRA) background.
- Experience deploying, configuring, calibrating, or validating data acquisition for clinical trial medical devices.
Culture & Benefits
- Full-time employment.
- Collaboration with global teams across the US, Europe, and APAC.
- Participation in a 24/7 global support model.
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