Medical Scientific Affairs Manager

Greece, Athens

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At Roche, we believe every employee makes a difference. We are passionate about transforming patients’ lives. We are fearless in both decision and action; we believe that good business means a better world. Organizational capacity to attract, motivate and retain talent is a vital element for balanced organizational success and innovation.

Main Activities:

In this role you will report to Head of Medical Scientific Affairs & Healthcare Development. You will be part of a high performing team with the ability to lead Roche Diagnostics Hellas Medical Scientific Affairs activities, namely on:

  • Medical Plan 
  • Medical budget
  • KOL engagement plan, strategy and tactics
  • Medical Information Management

Your main focus in this role is to:

  • Map and visit key stakeholders and build new relationships with national level key opinion leaders in assigned disease areas of responsibility
  • Develop and execute a medical plan incorporating to medical objectives, strategies and tactics
  • Develop and execute study strategies with health care professionals (“HCPs”), specifically responding to requests for information about Off-Label uses of RD products.
  • Design and deliver disease and product training for customers and marketing and other departments as required
  • Able to develop and execute non promotional scientific speaker programs, scientific advisory boards and scientific publications
  • Develop the Medical affairs function providing direction, coaching and development
  • Liaise with all relevant functions at Roche and specially align with local Regulatory & quality function

Who you are

The ideal candidate should possess the following requirements:

  • Ph.D. Degree in Health sciences or MD degree required
  • Minimum 3 years working experience in Biomedical/Pharma industry in Cardiac care (unless MD degree with specialization in Cardiology)
  • Knowledge of the overall use of in-vitro diagnostics
  • Strong interpersonal skills and customer service orientation
  • Excellent planning and organizational skills
  • Experience in development and implementation of clinical trials
  • Experience of writing clinical publications and deliver scientific presentations
  • Excellent relationships with external HCPs, KOLs
  • Excellent command in English language (verbal & written)
  • PC literate, excellent Windows & MS Office