Clinical Evaluation Medical Device

Location
Germany (DE)
Salary
Comprehensive
Posted
15 Jan 2021
Closes
11 Feb 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Clinical Evaluation Medical Device

I am currently partnered with a Global Medical Device company who due to continued success and the continuous efforts of the business to operate at the highest level, are looking to add a Clinical Evaluation Specialist to their team. If you have extensive experience within Clinical Evaluation, please keep reading.

Role

  • Responsible for literature research in the field of orthopaedics and sports medicine to identify literature-based evidence for clinical acceptance criteria
  • Working closely with the regulatory department to answer clinical questions
  • Creation and maintenance of the clinical sections of Clinical Evaluation Reports in line with MEDDEV 2.7 / 1
  • To support the preparation of study protocols
  • Analysis and Interpretation of clinical data, creation of summaries in the form of presentations and scientific texts
  • Regular coordination with global members of the research, product management, regulatory and additional contributors

Requirements

  • A degree in natural sciences, medical engineering, life science, MD
  • Minimum of 3 years experience in a comparable role
  • Conversant with MS Office programs, plus experience of statistical software such as SPSS or JMP
  • Strong understanding and proven application of requirements governing medical device sector (MDR, MDD, ISO 14155) with the preparation of clinical evaluations according to MEDDEV 2.7
  • Experience conducting literature research and study of databases (Pubmed, Embase, etc.)
  • Fluent English and strong German language skills, both spoken and written

Benefits

  • Comprehensive Package including Bonus
  • Flexible working hours
  • Company pension scheme
  • Supplementary health insurance
  • Lunch provided Monday to Friday

If you are interested, get in touch with me ASAP…

Dan Hockaday

Pharmacovigilance & Drug Safety Recruitment Consultant

Email: Dhockaday (at) barringtonjames.com

Phone: 00441293776644