NL-Medical Information & Compliance manager - 70000047
Passion for Innovation. Compassion for Patients.
With over 120 years of experience and more than 17,000 employees in over 20 countries, 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 strive to become a global pharma innovator with competitive advantage, creating novel therapies for people with cancer.
Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada.
Purpose of the function
The Medical Information & Compliance Manager is responsible for the internal and external medical information, and compliance with all applicable Dutch pharma CGR directives. This is done via medical training according to latest scientific information, via ensuring the scientific correctness and completeness of HCP- and non-HCP directed materials, and via providing answers to unsolicited requests for medical information. The Medical Information Manager assists the responsible for Information and Publicity oversight activities. The Medical Information & Compliance Manager reports to the Head Medical Affairs SBD NL. The position is a role for 20hrs/week. The Medical Information & Compliance Manager is expected to be at the office 2 days per week of 8 hours. The remaining 4 hours is expected to be applied in a flexible fashion over the remaining 3 days.
Roles and Responsibilities
Medical training :
The Medical Information & Compliance Manager organises the internal cardiovascular therapeutic area, indication, and product training in close collaboration with the medical affairs team.
Compliance
Total 6 hours/week · ToV reporting Transparency register and contact person in case of questions/inspection · CGR training onboarding and refresher · Being the CGR expert e.g. courses, newsletters ·Compliance meetings with legal and compliance · Transpharmacy approvals
Review of customer-facing material
The Medical Information & Compliance Manager assists the responsible for Information and Publicity for the review of customer-facing material (Cardiovascular and Oncology material).
Provide medical information to external customers
The Medical Information Manager organises customer-centric medical information in collaboration with all medical personnel involved in medical information activities for both Cardiovascular and Oncology. ◦
Skills and additional Requirements
• University Degree in Medical Science University degree in Medical Science, BioScience, or Pharmacy
• 2 to 5 years Professional experience in Medical Affairs Department, preferably in a similar role
• Experience in pharmaceutical or Biotech industry
• Knowledge and experience in Medical Literature analysis and conduct
• Eye for details
• Advanced communication and presentation skills
• Positive and proactive attitude
• Flexible
• Strong team spirit
• Skilful with Office programs
• CGR knowledge
Why work with us?