请问如何能索要赔偿# Law - 律师事务所
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PURPOSE
To support Philips Research Shanghai by running quality clinical research
projects. Clinical research projects are aimed to test “new to the world”
technologies that have the potential to transform healthcare as we know it
and will assist in defining the strategic direction taken by the company.
Additionally, candidate is expected to support Engineering, Regulatory or
Marketing needs within required regulatory and scientific framework
PRINCIPAL ACCOUNTABILITIES
- Develop technologies that will be used in a biomedical engineering system.
-Design, implement, test and improve both biomedical hardware and software
platforms in lab settings that demonstrate the performance of the new
technology.
- Maintains high throughput and work quality at research sites.
-Prepare and execute clinical tests for the new technology in the
collaborated hospital.
- Develop clinical trial protocols to include sound scientific procedures,
accurate timelines, and complete scientific references.
- Ensures research processes and procedures are state of the art and meet
all regulatory requirements.
MAJOR CHALLENGES
The task of the Philips Research organization in Shanghai is to research and
develop medical technologies and applications tailored for the China market.
To reach this purpose, we employ people with clinical trial competence and
technical competence, who work together in teams.
The major challenges for the candidate is to
1) Design, implementation, testing and improvement of both biomedical
hardware and software, instead of only perform algorithm research and
validate the algorithm
2) Be able to quickly ramp up in related medical field and gain
corresponding clinical domain knowledge, use the gained knowledge in system
development
3) Ensure quality data through sound scientific protocols, study execution,
study monitoring, and adherence to all regulatory requirements
4) Manage multiple parallel tasks while maintain ethic guidelines.
5) Manage multiple relationships – internal and external to complete tasks
successfully
JOB REQUIREMENTS
a) Education:
Excellent research experience in the field of biomedical engineering, as
demonstrated by having obtained a Masters degree or higher. The degree
should be supported by publications in renowned international journals.
b) Experience:
- Experience (2 years +) in working with biomedical system development.
Preferably experience in developing professional medical equipment, or where
you worked on HW-SW integration.
- Experience (2 years +) in clinical research preferably in the medical
device industry or field of sleep or respiratory medicine
- Demonstrated scientific writing experience
- Demonstrated efficiency with computer software for document preparation,
reports, presentations, communication, e-mail, and data management.
- General understanding of statistics
c) Competency and Skills:
Technical skills:
Practical experience in designing hardware platform
Practical experience in developing signal processing algorithms.
Excellent software development skills using practical languages such as
Matlab etc.
Architectural thinking and system design ability
Broader skills:
A quick learner and be able to apply the newly gained medical domain
knowledge in your work, in particular, in areas that not touched upon before
, such as medical/clinical knowledge
Social skills:
Drive, entrepreneurial behavior, result and quality driven. People focus.
Excellent communication skills. English language skills to at least CET
level 6.
Positive mindset.
Interested candidates please send your resume to Emily Qian at [email protected]
philips.com, and specify where you see this position advertised.
To support Philips Research Shanghai by running quality clinical research
projects. Clinical research projects are aimed to test “new to the world”
technologies that have the potential to transform healthcare as we know it
and will assist in defining the strategic direction taken by the company.
Additionally, candidate is expected to support Engineering, Regulatory or
Marketing needs within required regulatory and scientific framework
PRINCIPAL ACCOUNTABILITIES
- Develop technologies that will be used in a biomedical engineering system.
-Design, implement, test and improve both biomedical hardware and software
platforms in lab settings that demonstrate the performance of the new
technology.
- Maintains high throughput and work quality at research sites.
-Prepare and execute clinical tests for the new technology in the
collaborated hospital.
- Develop clinical trial protocols to include sound scientific procedures,
accurate timelines, and complete scientific references.
- Ensures research processes and procedures are state of the art and meet
all regulatory requirements.
MAJOR CHALLENGES
The task of the Philips Research organization in Shanghai is to research and
develop medical technologies and applications tailored for the China market.
To reach this purpose, we employ people with clinical trial competence and
technical competence, who work together in teams.
The major challenges for the candidate is to
1) Design, implementation, testing and improvement of both biomedical
hardware and software, instead of only perform algorithm research and
validate the algorithm
2) Be able to quickly ramp up in related medical field and gain
corresponding clinical domain knowledge, use the gained knowledge in system
development
3) Ensure quality data through sound scientific protocols, study execution,
study monitoring, and adherence to all regulatory requirements
4) Manage multiple parallel tasks while maintain ethic guidelines.
5) Manage multiple relationships – internal and external to complete tasks
successfully
JOB REQUIREMENTS
a) Education:
Excellent research experience in the field of biomedical engineering, as
demonstrated by having obtained a Masters degree or higher. The degree
should be supported by publications in renowned international journals.
b) Experience:
- Experience (2 years +) in working with biomedical system development.
Preferably experience in developing professional medical equipment, or where
you worked on HW-SW integration.
- Experience (2 years +) in clinical research preferably in the medical
device industry or field of sleep or respiratory medicine
- Demonstrated scientific writing experience
- Demonstrated efficiency with computer software for document preparation,
reports, presentations, communication, e-mail, and data management.
- General understanding of statistics
c) Competency and Skills:
Technical skills:
Practical experience in designing hardware platform
Practical experience in developing signal processing algorithms.
Excellent software development skills using practical languages such as
Matlab etc.
Architectural thinking and system design ability
Broader skills:
A quick learner and be able to apply the newly gained medical domain
knowledge in your work, in particular, in areas that not touched upon before
, such as medical/clinical knowledge
Social skills:
Drive, entrepreneurial behavior, result and quality driven. People focus.
Excellent communication skills. English language skills to at least CET
level 6.
Positive mindset.
Interested candidates please send your resume to Emily Qian at [email protected]
philips.com, and specify where you see this position advertised.
