Senior Medical Advisor Hematology at AstraZeneca
20157 Milano, Lombardia, Italy -
Full Time


Start Date

Immediate

Expiry Date

04 May, 25

Salary

0.0

Posted On

04 Feb, 25

Experience

0 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Legislation, English, Pharmaceutical Industry, Interpersonal Skills, Hematology

Industry

Pharmaceuticals

Description

Would you like to apply your expertise to make an impact in a company that follows the science and turns ideas into life-changing medicines? Then AstraZeneca might be the one for you!
At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve, no matter where you start with us.
Welcome to MIND (Milan), one of over 400 sites here at AstraZeneca. The site provides a collaborative environment where everyone feels comfortable and able to be themselves, which is at the core of AstraZeneca’s priorities.
As a global biopharmaceutical company, we are committed to advance the science of oncology to deliver life-changing medicines and make a positive impact on changing patients’ lives. In the last 15 years, AstraZeneca has built and strategically acquired one of the most promising Oncology pipelines in the industry. We are helping patients by redefining the cancer treatment paradigm in four main disease areas - breast, ovarian, lung and hematological cancers.

ESSENTIAL REQUIREMENTS

  • Previous experience as Medical Advisor/Medical Manager in the Hematology area within a Pharmaceutical company
  • Understanding of sales and marketing and pharmaceutical medical information
  • Knowledge of legislation relevant to pharmaceutical industry
  • Ability to manage incoming data and/or requests in a timely manner and escalate when appropriate
  • Strong leadership capabilities
  • Excellent interpersonal skills
  • Extensive experience in relationship and stakeholder management experience
  • Proficiency in English and Italian

DESIRABLE REQUIREMENTS

  • Qualified Doctor in Hematology/Oncology
  • PhD in Hematology/Oncology
Responsibilities
  • Reporting to the Therapeutic Area Lead Hematology, you will collaborate with different Company’s functions (e.g. marketing, sales, regulatory, training, market access and clinical research) in order to contribute to the development of medical strategies and provide high quality scientific support.
  • The role will include the following aspects:
  • Supporting the development of the Product Business Plan (PBP), ensuring alignment with HQ strategies and policies.
  • Contributing to the definition of the Product Business Plan (PBP), according to the HQ strategies and policies
  • Preparing the National Medical Plan on assigned product, defining strategies and objectives, according to the HQ strategies and policies
  • Providing expert training to the medical field team, enhancing their understanding of the product and disease landscape, and supporting the development of the local medical plan.
  • Advising the Field Force in communications with medical target groups by continuously updating them on therapeutic topics related to the pathology and/or products.
  • Ensuring the inclusion of Italian Centres to the international clinical development research(e.g.: by maintaining close contacts with the relevant international Product Teams)
  • Guaranteeing, with the Clinical Research Manager (CRM), the local implementation of global trials
  • Overseeing local study protocols, ensuring accurate data management and analysis, preparing final study reports and ensuring publication of data timely
  • Providing high quality of support to the Regulatory Affairs Dept in the definition and review of the product registration dossier and other documents
  • Providing support to Marketing Dept to guarantee the high scientific and educational standard in the relevant activities (e.g: preparation and review of promotional material; planning and organisation of scientific events)
  • Developing and maintaining a high level of scientific engagement with key Opinion Leaders and Scientific Community
  • Collecting and discussing with sponsors ESRs proposals and to collaborate with the MEOR manager according to AZ SOP
  • Managing all activities and Account relationship according with Company Values, Code of Conduct, Guidelines/Internal procedures and Italian legislation
  • Managing medical information requests
  • Overseeing medical information requests and managing all activities and account relationships in line with Company Values, Code of Conduct, Guidelines/Internal procedures, and Italian legislation.
Loading...