Global Program Medical Director
vor 1 Woche
**Global Program Medical Director (gn) - Oncology**:
- At MorphoSys, our ambition is to redefine how cancer is treated. As a global, commercial-stage biopharmaceutical company, we are driven by the urgency to discover, develop, and deliver groundbreaking medicines, aspiring to give more life for people with cancer.
- Our success is created by our people and we bring together exceptional talent from around the world. We are an equal opportunity employer and take pride in offering our colleagues an open, flexible, and diverse work environment. We are looking for people who share our values and are motivated to improve the lives of people impacted by cancer.-
**Your Responsibilities**:
- Responsible for developing and executing the Clinical Development Plan (CDP) for 1 indication in an oncology development program at MorphoSys
- Lead Medical Scientists in the department of Clinical Development
- Support GCPH (Global Clinical Program Head) and Sr GPMD with strategy and input to the Global Program Team and other teams on behalf of the Clinical Development Function
- Generate and execute the indication specific CDP in alignment with GCPH
- Develop and (co-)author high quality, feasible, comprehensive state-of the art study synopses and protocols and in close cooperation with Clinical Operations, other stakeholders (e.g. Statistician, Safety, etc) and clinical scientist
- Build or foster relationships within the appropriate clinical / scientific community
- Support the organization of effective Scientific Advisory Boards, and establish, maintain and leverage an international network of key opinion leaders for the given therapeutic area
- Write or review abstracts / manuscripts, etc. for presentation / publication at internal/external high rank meetings or congresses, support their placement in high impact journals
- Supervise Medical Scientists in Clinical Development during study set-up and conduct to ensure operational feasibility, continuous state of the art medical monitoring, medical management of investigative sites, inspection readiness at all times
- Support GCPH and Sr GPMD in leading the preparation of clinical / medical content for corresponding regulatory filings
- In close cooperation with Regulatory Affairs help to coordinate the contributions of other functions to the documentation, as well as interaction with regulatory authorities and payer / HTA bodies
- Support the medical and commercial organization with the necessary content
**Job Qualifications**:
- Physician with medical degree
- Strong background in oncology
- Patient treatment experience in clinical medicine, preferably in oncology
- Track record in drug development in clinical phases 1-4 including design, conduct, analysis and reporting / publishing of clinical trials
- Experience in interactions with Health Authorities (with emphasis on FDA/EMA)
- Successful team leadership and/or people management desired
- Proactive, dynamic personality, yet a team player
- Strong leadership skills, able to motivate and train other Clinical Development personnel to exploit their full capabilities
- Willingness and ability to work on a global scale
- Excellent presentation skills
- Strategic thinker
- Fluent in written and spoken English is a must
**We offer**:
- Creative working in X-functional teams
- Open and appreciative corporate culture
- Multicultural environment
- Working in an attractive, high-quality equipped building with restaurant
- Free sports and language courses
- MorphoSys AG, Semmelweisstraße 7, 82152 Planegg
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