Medical Scientist, Biologist - Clinical Scientist Oncology (m/f/d)

Beschreibung

MorphoSys’ mission is to make exceptional, innovative biopharmaceuticals to improve the lives of patients suffering from serious diseases. Innovative technologies and smart development strategies are central to our approach. Success is created by our people, who focus on excellence in all they do, collaborate closely across disciplines. We all are driven by a desire to make the medicines of tomorrow a reality. Guided by mutual respect and trust, each member of the MorphoSys team is given the opportunity to develop and flourish within this exciting and inspiring environment. Join us in Planegg near Munich!

We would like to fill the following vacancy as soon as possible:

• Responsible for providing medical / scientific input and expertise to individual clinical trial(s) within a global development program of a disease area
• For the assigned clinical trial(s) within program, as a member of the Clinical Trials Team, provide medical scientific input to: all activities related to planning, execution and reporting of clinical trials; development of trial related documents (e.g. protocols, case report forms, data analysis plan, reports, publications); development of presentation material for trial-related advisory boards, investigators meetings, protocol training meetings for CRO
• Ongoing review of clinical trial data, final analysis and interpretation, in collaboration with the Safety Leader and appropriate CTT members
• Build relationships among the clinical / scientific community and with external experts
• Represent Clinical Development in Clinical Trial Teams, participate and contribute in clinical subteams and other committees needing medical support
• Maintain sponsor oversight on data quality and product safety in clinical trials in collaboration with the Safety Leader and appropriate Clinical Trial Team members. Perform hands on medical data review, as needed
• Support regulatory authority interactions, information requests etc. as needed, and based on individual expertise, perform evaluations of potential drug targets and drug candidates for future clinical development
• No people management responsibilities

• Ideally MD, PharmD or PhD in health sciences / translational research with substantial experience in clinical development
• Strong background in haemato-oncology, oncology or immuno-oncology is preferred
• Experience in early or late drug development is preferred
• Ideally a minimum of three years of relevant professional experience with at least three years in the pharmaceutical or biotechnology industry
• Prior experience in regulatory authority interactions / submissions, either as lead or part of a team is preferred
• Ability to critically evaluate drug targets or drug candidates based on published data or preclinical research findings and to translate these findings into clinical hypothesis testing
• Excellent presentation skills
• Strategic thinker
• Fluent in written and spoken English is a must

• 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