Jr. Consultant Clinical Affairs Medical Devices 

Nanjing / Greater Shanghai / Beijing, China 

Minimum 2 years working experience in Medical Devices /
knowledge of Medical Device Regulations and/or Clinical Affairs

(Please find here the Chinese version of this vacancy).

Is this your DNA? 

Are you passionate to help customers? Are you able to find the right balance between business needs and quality of work in the interest of the customer, while always staying close to ethical and professional values and pride in the work that you deliver? Do you have a practical approach and being creative in finding pragmatic solutions within your projects for customers? Then please take a look at our career opportunities at Qserve. We would like to get in contact with you!

This is what you will be doing at Qserve:

As a Junior Consultant Clinical Affairs at our company you provide support in services around clinical evaluation, literature searches and clinical studies to our customers in the medical device industry. Together with colleague consultants, you contribute to clinical data collection, analysis, and reporting. In cases where the data is collected under a Clinical Investigation Plan, instructions regarding clinical data capture will have to be provided to the investigational sites following the GCP standard ISO14155. You will also gain experience in developing and executing clinical monitoring, appropriately and in a risk-based manner. Writing clinical reports will be(come) your key competence! You will pro-actively follow the news and trends in the market to share within our Knowledge Center In your expertise area, you will be responsible for writing blogs, whitepapers, news items, presentations or similar to promote knowledge base and the Qserve brand. 

And this is what you will bring:

You have a technical or scientific degree (MSc or PhD) in physics, mechanical engineering, chemistry, (medical) biology, biomedical technology or similar. 
Minimal 2 years working experience in the field of medical devices or pharmaceuticals through positions in industry, consultancy or clinical research organizations (CRO), in either clinical research associate (CRA), R&D, clinical, quality or regulatory roles. 
Knowledge of Medical Device Regulations (CE, FDA, PAL, TGA, etc.) and/or Clinical affairs. 
Pragmatic, enjoying a mix of activities in technology, business processes and Clinical affairs.
Communicative and service oriented, supporting a wide variety of clients from small start-ups to large multi-nationals, able to adapt to different company cultures and situations.
Strong organizational skills, detailed oriented to deal with various projects at the same time.
Fluent in English. 

“Global reach, practical approach, experienced team”


Getting excited about a career as a consultant in the dynamic and innovating world of medical devices? Then please submit your resume and letter of motivation to careers@qservegroup.com or use our application form. For more information about our company, you can always visit our website or reach out to Stephanie Huang at Stephanie.huang@qservegroup.com or call at +86 133 05 15 29 92.

The function may be partly home-based; we expect our consultants to work at the client locations, from home and/ or from Nanjing office, depending on the need.

Enquiries from agencies are not appreciated.

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