Medtronic te jobs (salary & requirements)

Job Description fSeniMedical Writer
1. Job Scope
1). Regulatory Writing
Write EU MDR Clinical Evaluation Report (CER), Clinical Evaluation Plan (CEP), Summary of Safety Clinical Performance (SSCP), Postmarket Clinical Follow-up (PMCF) plan report.
2). Scientific Writing
Write abstracts posters fconferences. Write manuscripts to be published in peer-reviewed international journals.
3). Other Writing
Write medical documents fscientific marketing, such as Clinical Experience Papers.
Must-have skills education/training background
1. Master of Science degree in biomedical/clinical science, Ph.D. is preferred.
2. At least 3 years of biomedical/clinical research experiences
3. At least 3 years of medical writing experience.
4. Familiar with the regulatory guidance polices of China NMPA EU MDR
5. Understbiomedical/clinical literature
6. Excellental written communication skills
7. Excellent communication strong collaboration with Regulatory Affairs, Quality Control team investigators
8. Sensitive to project timeline
9. Excellent project management skills
10. Understclinical study design, biostatistics, biomedical/clinical science.
11. Extensive experiences in scientific writing have published a minimal of 3 research papers in peer-reviewed international journals.
12. Database management experience in the Administratcapacity (Quosa, equivalent)
13. Experience managing Endnote Libraries
14. Fluent in written English Chinese