Job Description
Mitsubishi Tanabe Pharma GmbH (part of Mitsubishi Chemical Group).Hybrid working (3 days in office, 2 days remote)
At Mitsubishi Tanabe Pharma our clinical research operations have been established in Europe since 2001 and we are currently supporting the development of compounds in several disease areas. Medical Affairs is a unique organization within MTPD that focuses on the communications between the company and medical professionals, healthcare providers, health insurances, and patients.
Your primary role will be to act as Deputy Qualified Person (GDP-related) and Deputy Graduated Plan Officer (GVP-related), and to communicate scientific and clinical information. You will cooperate cross functionally with clinical research, marketing and sales, market access, pharmacovigilance, regulatory affairs, as well as other departments within the organization, providing medical clinical advice for business development. You will develop strategic medical plans including publication plan, data dissemination, health care professional engagement, data generation and life cycle management.
Your responsibilities:
- Provide medical support for launches in numerous European countries, both, in the hospital and retail market.
- Ensure team members are properly trained, and medical concepts and projects (including Investigator Initiated Studies (IIS)) are implemented in line with the current therapeutic area medical plan/strategy.
- Identify and profile treating centers and support understanding of the patient journey from the occurrence of first symptoms to first treatment as well as patient transition journey from hospital setting to patient's home.
- Contribute through Field Medical Affairs to the initiation, conduction, evaluation, and reporting of clinical projects including Phase III and IV studies, Handling of Investigator Initiated Projects including review and approval and Local NIT/PMS (non-interventional trial / post marketing survey).
- Prepare, review, approve and conduct communication material, medical information, educational and training programs.
- Conduct congress activities such as scientific symposia, abstract and poster presentations and gather scientific knowledge.
- Prepare and conduct advisory boards and scientific meetings to expand the understanding of the broad clinical and scientific community needs.
Your Qualifications and Skills:
- Scientific or medical qualification essential e.g. Medical Doctor or Master's degree in Natural Sciences; Doctorate degree preferred.
- Qualified to take over the responsibility as Deputy Qualified Person (“Grosshandelbeauftragter”) according §52a German Drug Law (GDP-related) and Deputy Graduated Plan Officer (“Stufenplanbeauftragter”) according §63a German Drug Law (GVP-related).
- Proven experience in medical affairs and as a medical scientific liaison manager or similar (field experience is desirable), ideally in CNS, hospital and community services for CNS patients and rare disease indications.
- Knowledge of appropriate data bases (e.g. Medline).
- Good working knowledge of German and ideally other European medical environment practices.
- Fluent in English, additional major European language advantageous, especially French.
Our corporate culture is based on the values of integrity, respect, bravery, collaboration, and persistence, we call it "Our Way". With our approach, together we can shape a more sustainable, progressive, and brighter version of the world. We believe in the power of people with diverse values, viewpoints, and expertise. Our aim is the wellbeing of people and the planet – a concept we call KAITEKI. We are committed to creating an inclusive and diverse environment.View More