GE HealthCare Medical Advisor 

Japan, Chiyoda 

39116640

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, especially in the Nuclear Medicine, Radiology, Oncology, Neurology or Gastroenterology.

Involvement in the assessment and monitoring of investigator initiated trials.

Preparation and delivery of training and education on new industry campaigns and clinical evidence.

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:

Pharmacist, or in pharmacy, agriculture, and other science.

Approximately 2 years exprience in a medical affairs or R&D in industry with experience of approving promotional materials in accordance with the appropriate regulations

Study management under the clinical trials act in Japan.

Well trained in compliance and Japanese code of practice.

Preferred Qualifications:

Medically or pharmaceutically qualified and registered, such as M.D., Ph.D, Master degree,

Self-motivated with a proven ability of working to deadlines

Experience in any of Nuclear Medicine, Radiology, Oncology, Gastroenterology or Neurology preferred.