應屆畢業生
本科
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職位描述
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Responsibilities
1. Manage the clinical evaluation of our products for their release and launch to the global market.
a. Manage and perform gap analysis for new product clinical performance and advise project team on clinical evaluation requirements
b. Responsible for the evaluation of clinical data for new product clinical evaluations.
c. Responsible for post-market clinical follow up plan and strategy.
2. Responsible for the clinical lifecycle throughout the lifecycle of SSMR product portfolio.
a. Continuously monitor and verify the device’s clinical performance and safety as part of post-market clinical follow up
3. Responsible for the Clinical Evaluation and Clinical Lifecyle Management process according to Medical Device Regulation and NMPA regulations. Working closely with counterparts in Erlangen and quality department to establish a harmonized process.
4. Post market clinical follow up process at SSMR and will work closely with project teams in SSMR and counterparts in Erlangen.
5. Responsible for the product Survey and Analysis report of SSMR products to ensure that market feedback is incorporated into our product development.
6. Responsible keeping up to date with latest regulatory body clinical evaluation requirements and standards and incorporating them into our process and lifecycle management
Requirements
-Good level of English language skills both spoken and written
-Qualifications: Clinical / medical degree
-Knowledge of regulatory requirements (EC DoC and NMPA highly desirable)
-Strong communication skills bringing stakeholders and 3rd party together to perform the clinical evaluation and management
-Good organizational and leadership qualities
-Proactive "getting things done" attitude
-Experience of liaising with medical opinion-leaders, specialist associations, funding bodies and politicians, ideally having a network within relevant specialist committees (highly desirable).
-Highly results-oriented with a growth mindset. Capable of presenting action to management and/or customers.
-Work experience within a multidisciplinary and multicultural environment (highly desirable).
1. Manage the clinical evaluation of our products for their release and launch to the global market.
a. Manage and perform gap analysis for new product clinical performance and advise project team on clinical evaluation requirements
b. Responsible for the evaluation of clinical data for new product clinical evaluations.
c. Responsible for post-market clinical follow up plan and strategy.
2. Responsible for the clinical lifecycle throughout the lifecycle of SSMR product portfolio.
a. Continuously monitor and verify the device’s clinical performance and safety as part of post-market clinical follow up
3. Responsible for the Clinical Evaluation and Clinical Lifecyle Management process according to Medical Device Regulation and NMPA regulations. Working closely with counterparts in Erlangen and quality department to establish a harmonized process.
4. Post market clinical follow up process at SSMR and will work closely with project teams in SSMR and counterparts in Erlangen.
5. Responsible for the product Survey and Analysis report of SSMR products to ensure that market feedback is incorporated into our product development.
6. Responsible keeping up to date with latest regulatory body clinical evaluation requirements and standards and incorporating them into our process and lifecycle management
Requirements
-Good level of English language skills both spoken and written
-Qualifications: Clinical / medical degree
-Knowledge of regulatory requirements (EC DoC and NMPA highly desirable)
-Strong communication skills bringing stakeholders and 3rd party together to perform the clinical evaluation and management
-Good organizational and leadership qualities
-Proactive "getting things done" attitude
-Experience of liaising with medical opinion-leaders, specialist associations, funding bodies and politicians, ideally having a network within relevant specialist committees (highly desirable).
-Highly results-oriented with a growth mindset. Capable of presenting action to management and/or customers.
-Work experience within a multidisciplinary and multicultural environment (highly desirable).
注：聯系我時，請說是在江蘇人才網上看到的。
工作地點
地址：深圳南山區南山區高新中二道32號西門子磁共振園
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詳細位置，可以參考上方地址信息
求職提示：用人單位發布虛假招聘信息，或以任何名義向求職者收取財物（如體檢費、置裝費、押金、服裝費、培訓費、身份證、畢業證等），均涉嫌違法，請求職者務必提高警惕。
職位發布者
SSMR..HR
西門子(深圳)磁共振有限公司
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批發·零售
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200-499人
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外商獨資·外企辦事處
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高新中二道32號高新中二道西門子磁共振園
