Medical Oncology Specialist

4 settimane fa

Roma, Lazio, Italia AbbVie A tempo pieno
Job Description

As a Medical Oncology Specialist at AbbVie, you will play a crucial role in driving medical activities to support the Brand Strategy and integrate it into the Brand Plan. Your expertise in oncology will be essential in warranting the medical know-how of the Affiliate regarding the relevant therapeutic areas of assigned products.

Key Responsibilities:

  • Drive medical activities to support the Brand Strategy and integrate it into the Brand Plan.
  • Represent the Italian Affiliate in the relevant therapeutic Corporate Medical Development setting.
  • Prepare the medical plan of activities for each product of the relevant area, on an annual basis and to update it as appropriate.
  • Contribute to the design and improvement of AbbVie Medical Department Italy (AMDI) systems and processes.
  • Manage the budget of the relevant therapeutic area, including local clinical studies.
  • Design local AMDI clinical studies and review, approve, and fulfill contract agreements of Investigator Initiated Studies (IISs).
  • Foster the participation of the Affiliate to International clinical trials and provide comments on the design and implementation of International protocols.
  • Identify potential sites for carrying out International and local clinical studies and maintain a liaison with them throughout the study conduct.
  • Maintain a continuous relationship with Key thought Leaders and External Experts in the relevant therapeutic area.
  • Address queries by physicians regarding the relevant products and provide medical support on marketed products to the Pharmacovigilance Unit.
  • Design or participate in the design of AbbVie events, warranting an appropriate medical support to the Commercial Divisions.
  • Provide medical-scientific updates on TA, products, and competitors, as agreed with the Commercial Divisions.
  • Review promotional material and the Summary of Product Characteristics and Insert Leaflets, prepared by Regulatory Affairs.
  • Support the Scientific Training Specialist(s) in preparing the annual scientific training plan for the sales force.
  • Provide medical support to the Pharmacovigilance Unit as to AEs reported in clinical trials on the relevant products.

Qualifications:

  • Medical or master's degree in life science related subjects.
  • Minimum of 3 years' working experience in clinical context or in pharmaceutical/biotechnological industry, in a scientific/medical role, within cross-functional teams.
  • Minimum 2 years of experience in oncology, with experience in onco-gynecology and companion diagnostics being a plus.
  • Ability to transform strategies into feasible and realistic actions.
  • Ability to lead, motivate, and coordinate cross-functional teams.
  • Excellent knowledge of the health sector and its development.
  • Effective management of work in a matrix structure.
  • Knowledge of financial principles and processes.
  • Fluency in written and oral English (Minimum Common European Framework Level: C1).

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