Clinical Scientist (gn) in Clinical Development

scheme imagescheme imagescheme image

MorphoSys’s 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, collaborating 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!

Your Responsibilities:

  • Responsible for providing medical / scientific input and expertise to individual clinical trial(s) within a global development program of a disease area
  • Represent Clinical Development in Clinical Trial Teams (CTT), participate and contribute in clinical subteams and other committees needing medical support
  • For the assigned clinical trial(s) within a program, as a member of the CTT, provide medical and 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, investigator meetings, protocol training, etc.
  • 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
  • Maintain sponsor oversight on data quality and product safety in clinical trials via regular medical monitoring activities 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 (e.g. FDA and EMA) as needed
  • Based on individual expertise, perform evaluations of potential drug targets and drug candidates for future clinical development
  • No people management responsibilities

Job Qualifications:

  • Ideally PharmD or PhD in health sciences / translational research with substantial experience in clinical development and clinical research
  • Strong background in haemato-oncology, oncology or immuno-oncology
  • Experience in early and/or late drug development (Phase 1-3)
  • Ideally at least three years of relevant professional experience, ideally in the pharmaceutical or biotechnology industry
  • Prior experience in regulatory authority interactions / submissions preferred but not a must
  • 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 medical writing and presentation skills
  • Strategic thinker
  • Proficient 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

Thank you for your interest! We are looking forward to receiving your pertinent application documents. For your application please use exclusively our career portal. We offer not only excellent career prospects, but also support you from the very beginning – even helping you move if necessary.

MorphoSys AG, Semmelweisstraße 7, 82152 Planegg