Director Medical Information Oncology EUCAN (m/f/x)

 

Passion for Innovation. Compassion for Patients.

 

With over 120 years of experience and approximately 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.

In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.

In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.

Our European headquarters are in Munich, Germany, and we have affiliates in 14 European countries and Canada.

 

 

We are seeking highly qualified candidates to fill the position:

Director Medical Information Oncology EUCAN (m/f/x)

The Position:

The Director Medical Information Oncology EUCAN leads the Medical Information efforts of DS for its own and partnered products in Europe and Canada. The job holder will ensure the highest standard of customer service where quality of responses and turnaround time are concerned whilst maintaining compliance with DS and potentially relevant partner SOPs. The position holder will ensure collaboration between the DS countries Medical Information services and the region to ensure the above and below deliverables and furthermore also support  the Senior Manager Medical Information who is tasked as Information Officer and help them in decision making, cover for absences etc. 

Roles and Responsibilities:

• Implements the European Oncology Medical Information Plan (including process and implementation plan for European-aligned Medical Information Systems and Services):
  • Ensure that all European Oncology medical information functions are capable to provide responses across the therapeutic area, in line with strategy, that the responses are of the highest quality, respond appropriately to HCP and other stakeholder inquiries, and are delivered to the customer in a timely fashion within the agreed turn-around-times.
  • Development, approval and sharing of European Standard Response Documents in Oncology
  • Support and lead (where instructed) Medical Operations activities in the Medical Affairs department.
• Proactively plans, develops and maintains the European Medical Information System and the reporting thereof:
  • Ensure requirements for update of European Medical Information system, based on change in healthcare and technological environment, are taken into consideration and improvements are implemented in cost efficient manner.
  • Improve processes, based on analytics on system usage.
  • Update existing reports and plan additional reports where required.
• Coordinates and align all MI activities and transfer of knowledge between Daiichi Sankyo Europe and other regions In Oncology and aligns processes with  Cardiovascular therapeutic area
  • Continue to leverage Medical Information Oncology expertise within the Daiichi Sankyo organization (e.g., sharing response documents with other business units as well as co-promotion/marketing partners) and proactively reach-out to similar medical information functional groups within the corporation to ensure cooperation and minimize redundant efforts.
  • Conduct regular trainings on Medical Information processes and content.
  • Support and lead the implementation of External and Internal Medical education activities, e.g. symposiums, Continuous Medical Education (CME) programs, MSL training activities, etc.
• Manages and supports the Senior medical manager Medical Information/ Information Officer 
  • Supports the Information officer in his/her/their task to ensure compliance under AMG 74
  • Supports the Information officer as needed in discussions with other reviewers and job owners 
  • As required e.g. during peak work load and absences , takes a hands-on role in signing off documents

Education & Professional Experience:

• Life science (at least master level) or medic