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Medical Director

2 mesi fa

Milano, Lombardia, Italia Kyowa Kirin A tempo pieno
Overview

We are pushing the boundaries of medicine at Kyowa Kirin International, where our purpose is to make a difference every day for those who need it most. Our culture is rooted in our values: Teamwork, Commitment to Life, Innovation, and Integrity. We take time to understand what matters to our patients, their families, and healthcare professionals, helping our people to take bold actions that deliver life-changing solutions sooner.

Responsibilities

As a Medical Director, you will provide optimal medical and scientific support across the Cluster, both externally and internally. You will be responsible for developing the medical strategy through the Medical Plan, aligned with the company strategy, and for coordinating the cluster oncology team with operational day-to-day oversight of the SRMs.

  • Develop and implement the medical strategy through the Medical Plan, aligned with the company strategy.
  • Coordinate the cluster oncology team and provide operational day-to-day oversight of the SRMs.
  • Build and maintain a professional network with relevant members of the medical/scientific community, pharmaceutical organisations, patient associations, insurance companies, and other applicable institutions.
  • Obtain and maintain in-depth knowledge on all aspects of the relevant KKI product(s).
  • Communicate balanced, substantiated, and relevant scientific information for internal and external stakeholders.
  • Final sign off of marketing materials.
  • Creation and/or review of medical materials, e.g., literature reviews, medical letters, slide kits, etc.
  • Input into cross-functional deliverables such as Regulatory Affairs (SmPC updates, DHCP letters, letters to competent authorities) or Market Access (dossiers, tenders, etc.).
  • Execute Risk Management Plan if applicable.
  • Facilitate publication of relevant local scientific and/or patient management data on KKI products.
  • Liaise with local patient organisations to find out about patients' needs and required patient support.
  • Give input into EMEA issues and projects.
  • Ensure appropriate response to unsolicited scientific requests by HCPs for licensed products/brands (on and off label), and for products in development in different clinical trials phases, by providing accurate scientific data in compliance with company policies, and country-specific legal and ethical requirements.
  • Develop KOL engagement plans and associated patient value insights and outcomes.
  • Actively develop agendas for, and participate in, advisory board meetings and clinical investigator meetings.
  • Facilitate expert lectures and external expert speakers with national, regional, or global recognition.
Qualifications
  • Relevant medical/pharmacy/nursing/bioscience background (higher degree preferred).
  • Knowledge of Regulatory Affairs, legal, and compliance regulations and authorities nationally.
  • Extensive experience in Medical Affairs Department.
  • In-depth knowledge of local, regional, and national healthcare systems and processes for allocation and delivery of care.
  • Track record of successful working with cross-functional teams locally and internationally.
  • High proficiency in English.
  • Well-developed interpersonal and communication skills with the ability to understand healthcare professional prospective and forge long-term relations of mutual value.
  • Acts as a role model for others in line with Kyowa Kirin culture and values.
  • Pharmaceutical Industry Acumen.
  • Research Methodology and Clinical Biostatistics.
  • Local and International Pharmaceutical Legislation, Sanitary Legislation. Good Clinical Practices and Pharmacovigilance.
  • Therapeutic areas and company products.
  • IT Tools and Database Medical Management Systems.
Options

Kyowa Kirin International is an equal opportunities employer. If you require any additional support through the interview process, you can raise this in complete confidence.