Medical Advisor Hematology- Italy

Career Category

Medical Affairs

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

Do more with the knowledge you’re working hard to acquire and the passion you already have. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Through this program, you will acquire the valuable hands-on skills and foundational experience to become the professional you are meant to be in your chosen field.

MEDICAL ADVISOR – HEMATOLOGY ITALY

                                             

LIVE

This could be your everyday

Let’s do this. Let’s change the world. In this vital role you will:

• Be responsible of Products lifecycle management ​
• Lead and develop the Local Medical strategy and Medical activities for the products in accordance to internal and external regulations​
• Actively involved in educating the scientific community through therapeutic area and product-focused medical training
• Manage internal and external relationships within area of responsibility​
• Ensure consistency of Medical content and scientific messages across various tools and materials​
• Support and execute Local study protocol preparation, filing, review and approval in line with Amgen processes and policies​
• Participate in the development of International strategies and tactics in close collaboration with the Globe Medical Affairs Lead
• Visit selected KOL’s and study groups for strategic discussions and protocol development​
• Review Local ISS proposals prior to approval and ensures appropriate Local review prior to IPRC submission, if applicable​
• Partner with the BU Manager in the development and execution of the Local products lifecycle management plan​
• Provide input into site selection for AST’s ​
• ​Participate in/conducts Local Advisory Board Meetings, Investigator Meetings and/or Expert Panels​
• Provide Medical expertise for Health Economy and reimbursement requests​

Outputs

• Brand/disease specific parts of Local R&D plan​
• Local support for Medical questions, feasibility and trial strategy​
• Local Product Lifecycle Plan ​
• Medical expertise for the review of promotional and scientific documents (e.g. symposia, publications etc.)​
• Local R&D brand/disease related results according to goals and metrics​

WIN

Here’s what it takes to Win

We are all different, yet we all use our unique contributions to serve patients. We seek a candidate with these qualifications.

• Relevant professional experience (typically around 5 years) in Scientific/Medical Affairs within the pharmaceutical/biotechnology industry or in a related medical/scientific field. This may include a combination of industry experience (e.g., Medical Science Liaison roles) and academically-based experience such as PhD, post-doctoral research, clinical training (residency/fellowship) with demonstrated application to Medical Affairs activities
• Medical education or deep scientific expertise in Hematology.
• Experience in a medically-related field can include post-doctoral training (i.e., residencies and/or fellowships)
• Experience in affiliate Medical Department or Clinical Development​

Preferred Requirements

• Knowledge of pharmaceutical product development, product lifecycle and commercialization process with advanced understanding of other functions (including, but not limited to, Clinical Operations, Commercial, Regulatory, and Medical Affairs​)

• Hematology area knowledge ​
• Network of customer contacts in therapeutic area​
• Finance and budgeting experience​

Competencies

• Medical and scientific expertise in Hematology
• Fluency in English, both oral and written communications
• Strong project management and presentation skills
• Continuously expanding medical and scientific knowledge as well as market knowledge
• Strong customer orientation; science-based 
• Ability to work in a cross-functional team (e.g., Commercial, Clin Development, EU teams, HE, Regulatory, Safety, etc.)
• Good knowledge of clinical research, drug safety, legal and compliance environment;
• Willingness to continuously expand medical, scientific, market, and industry knowledge,
• Science Based attitude, data driven, outside-in thinking and strategic overview;
• Result-driven and set to achieve goals;
• Patient centric and influential;

THRIVE

Some of the vast rewards of working here

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

• Vast opportunities to learn and move up and across our global organization
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

APPLY NOW

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

.