Match score not available

Medical Advisor Japan

extra holidays

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Japan

Offer summary

Qualifications:

2 years experience in medical affairs or R&D, Experience in Nuclear Medicine, Radiology, Oncology, Cardiology or Neurology, Oral and written communication in Japanese and English, Medically or pharmaceutically qualified (M.D., Ph.D., Pharmacist), Trained in compliance and code of practice.

Key responsabilities:

Lead the development and execution ofMedical strategies
Manage relationships with Key Opinion Leaders (KOLs) in relevant fields
Handle medical queries from healthcare professionals timely
Prepare and deliver education for industry campaigns and clinical evidence
Create and revise quality assurance documentation

GE Healthcare Large

10001 Employees

See more GE Healthcare offers

Job description

Job Description Summary

The Medical Advisor is a key partner to medical value through acting as the medical expert for key pharmaceutical products in Japan and also working with international medical affairs team.

Description

Job Description

The Medical Advisor is a key partner to medical value through acting as the medical expert for key pharmaceutical products in Japan and also working with international medical affairs team.

担当製品・領域のメディカル戦略の策定・実行をリードする役職です。医学専門家（KOLs）と教育セミナーや研究等を実施する他、コールセンターで回答できない社外からの問い合わせにも対応して頂きます。

Duties Include (but Are Not Limited To)

Developing and executing strategic medical plan of allocated products and therapeutic area.
Key contact point for relationships with Key Opinion Leaders (KOLs), especially in the Radiology, Nuclear Medicine or Cardiology.
Involvement in the assessment and monitoring of investigator initiated trials.
Managing medical queries from HCPs via call center, emails or sales team and take responsibility to rely in timely and compliant manners.
Preparation and delivery of education on new industry campaigns and clinical evidence.
Creating Q&A and revising timely, collaborating with global medical information. Provide scientific review on commercial materials.

Quality Specific Goals

Complete PV/PMS Quality & Compliance training within the defined deadlines.
Identify and report any quality or compliance concerns and take immediate corrective action as required.

Qualifications

Approximately 2 years experience in a medical affairs or R&D in industry with experience of approving promotional materials in accordance with the appropriate regulations.
Good collaboration skill with KOLs and internal cross functional team.
Well trained in compliance and Japanese code of practice.
Experience in any of Nuclear Medicine, Radiology, Oncology, Cardiology or Neurology.
Oral and written communication skills in Japanese and English (business level).

Preferred Qualifications

Medically or pharmaceutically qualified and registered, such as M.D., Ph.D, Pharmacist, or in pharmacy, agriculture, and other science.
Study management under the clinical trials act in Japan.
Self-motivated with a proven ability of working to deadlines.
Ability to work effectively in cross functional and cross border teams.

Additional Information

Relocation Assistance Provided: No