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Medical Adviser Oncology
Тип контракта
Полный рабочий день
Опыт работы в фармацевтической области
Более 6 лет

МОСКВА

Medical Adviser Oncology

Опубликовано: 15 Ноя 2021

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Responsibilities:

  • Development and implementation of strategy on TAs (Country Medical Affairs Plan for the year) and the provision of medical support within the life cycle for their responsible TAs and products in collaboration with colleagues from HH, including budget planning.
  • Engagement in scientific exchange with scientific leaders and key decision makers and collection scientific insights for the respective TAs.
  • Ensuring timely entering and monitoring scientific interactions and activities of scientific leaders engagement in Veeva Medical CRM during the year.
  • Providing, as necessary, written or verbal recommendations to HH colleagues on medical and scientific inquiries.
  • Conducting review and approval of promotional materials in accordance with the standard operating procedures of the Company.
  • Development and implementation of a continuing medical education program (CME), participation in the preparation and conducting of educational medical and scientific activities as part of regional or national events.
  • Conducting medical trainings per request providing informational support in relevant therapeutic areas.
  • Identify the unmet medical need in local clinical research in respective TAs, develop the concept and communicate with Regional and Global council.
  • Participation in congresses (international and national) as a representative of the medical department.

Requirements:

  • Advanced degreed professional (Medical or Biological Degree).
  • Oncology experience.
  • PhD degree in respective therapeutic area is a plus.
  • Ability to peer-to-peer communication and interaction with medical society representatives and scientific leaders.
  • Excellent ability to work with medical professional information, good analytical skills.
  • Ability to work effectively in a matrix’s organization both in team and on individual basis.
  • Familiar with clinical trials and non-interventional studies, scientific principles, marketing and have a knowledge of clinical trial design, strength in research and interpretation of medical data.
  • Medical and scientific writing skills.
  • Familiar with all aspects of product development, GCP and local regulations, including regulations of promotional materials; familiar with marketing principles and strategies.
  • Result-oriented, excellent communication and presentation skills.
  • Fluent English (Upper-Intermediate).

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