Clinician

Clinician, Health Care, European Medical Device Regulation, Clinical documentation, English

Your new company
nternational service corporation focusing on testing, inspection and certification for the safety of the world.

Your new role
Clinical expert with following duties:
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time
RESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time

RESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-timeRESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time

What you'll need to succeed
• Physician with completed medical degree
• Fluency in written and spoken English
• Ability to create qualified deficiency reports
• Experience working with MS Office applications and programs
• Excellent organizational and professional communication skills
• Ability to work in a team, pronounced customer orientation and good self-organization
• Curiosity and willingness to learn
• A total of at least four years of professional experience in the field of
o clinical practice in health care services or related sectors including two years in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices
• Experience with scientific literature searches in the medical context

What you'll get in return
• Full home-office
• Opportunity to work for global leader in audits
• Atractive salary
• International environment

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1172018
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Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Czech Republic
Specialism
Pharma
Ref:
1172018

Talk to a consultant

Talk to Aneta Valtova, the specialist consultant managing this position, located in Prague
Hays Czech Republic, Olivova 4/2096

Telephone: +420 608 160 049