||LILLY, one of the the world’s ten biggest pharmaceutical companies, is looking for a Medical Doctor in Rheumatology for the Medical Affairs Business Unit in the Rheumatology/Immunology Area. This professional can be based in Madrid or other affiliates of Europe (Paris, Basingstoke, Frankfurt, Florence, Brussels, Geneva, Amsterdam, Vienna, Copenhagen, Oslo, Stockholm, Helsinki, Warsaw, Prague or Budapest).
REPORTS TO: Therapy Area Leader (Rheumatology – BioMedicines)
MAIN FUNCTIONS AND RESPONSIBILITIES:
-Provide Medical Expertise and training for the cross-functional Rheumatology team
-Input into regulatory submissions and Health Technology Assessments (HTAs)
-Support / assist in the preparation of regulatory reports, preparation for regulatory agency advisory committee hearings and label discussions, local registration efforts, and communication and resolution of regulatory issues, including regulatory response, from an affiliate/country perspective
-Provide medical support for pricing, reimbursement and access (PRA)
-Conduct, coordinate and follow up of the evidence sharing plan
-Med Info support, scientific dissemination plans and product medical strategy plan.
-Contribute to the development, review and approval of the scientific information that has to be shared.
-Ensure the compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals.
-Provide presentation to groups of KOLs / HCPs and others as determined by business needs
-Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders (KOLs), and the general medical community on a local, national, regional, and possibly international basis.
-Support the planning of symposia, advisory board meetings, and/or the facilitation of other meetings with health care professionals.
-Participate in advisory committees.
-Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes / Real World Evidence and global PRA, clinical management or personnel and other cross-functional management within the affiliates during the development of the business plan.
-Contributing to the global and/or regional clinical/medical plan in rheumatology, conducting and reporting of clinical trials.
-Coordination and support for implementation of global clinical trials conducted in our region
-Collaborate in the development of protocols and data collection requirements.
-Medical Doctor in Rheumatology.
-Fluent in English, both written and verbal (Certificate in Advanced English / C1 Level).
-Proven experience in clinical practice and clinical research.
-Medical Affairs launch readiness and pharmaceutical medicine experience preferred.