Manager Clinical Research - Dentist

Posted 15 November 2021
SalaryNégociable
LocationLe Vaud
Job type Permanent
DisciplineLife Sciences
ReferenceBBBH493993_1636992273

Job description


For its partner specialized in Medical Devices, Kelly Life Sciences is looking for a:

Manager Clinical Research - Dentist
(Permanent position)

Your mission:
· You will support New Product Development and product maintenance activities
· You will also provide clinical and scientific insights and support regarding Clinical Research and Affairs

Your responsibilities:
· Contributes to clinical design input, Product Requirement activities, Validation and Verification planning and execution
· Approves Product Change Orders as the clinical representative at the site
· Provides clinical input to Quality Assurance regarding product complaints and Health Hazard Evaluations when necessary
· Organizes and executes Internal and External /Professional Product Evaluations
· Plans and implements User Evaluations
· Actively engages with the Procedure team to develop Voice of Customer insights
· Provides clinical support for the review and approval of Instructions for Use
· Contributes clinical Input for the planning of clinical studies, in-vitro studies, Investigator Initiated Studies, and PMCF
· Supports Clinical/Regulatory Compliance with clinical expertise
· Engages with the Procedure team to provide with Scientific and Clinical Support such as Scientific Clinical Communication, Scientific Manuals, Literature Reviews, and White Papers
· Assists with planning and delivery of product launch support materials such as, digital images and/or Video content for clinical compliance
· Support in the creation and review of technical files
· Support in the review of documentation (labelling)

Your Profile:
· Master's degree or equivalent in dentistry or other related science; A PhD or Certified Registered Dentist would be a plus
· Minimum of 3 years of clinical experience - Knowledge of clinical dentistry
· Experience in Medical Device Industry and product development
· Very good knowledge of European Regulatory rules (MDR) and US (21 CRF) concerning medical devices, FDA
· Experience in Medical Writing
· Fluent in English - Good knowledge of French would be ideal
· Strong interpersonal skills with the ability to build great relationships with multiple stakeholders
· Strong service- and customer-orientation
· Very good organizational and planning skills

Your contact at Kelly:
Mrs Karine Legerot
Consultant Professional Staffing Life Science
Kelly Life Sciences Geneva