Medical Advisor Cvrm

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.
Our aim is to protect the lives of 50 million people in the next year from the often-devastating consequences of heart failure, cardiovascular, metabolic and renal diseases.

Reporting to the Medical Area Lead, the Medical Advisor
- CVRM Amyloid Diseases, will be a key leader in further developing the “best in class” Specialty Care capability at AstraZeneca focusing on patients with severe amyloid driven diseases. Based on an extensive understanding of the unmet medical need, you will take a leadership role in defining the medical strategy and tactical plans in partnership with senior leaders.
If you’re inspired by the possibilities of science to make a difference and ready to discover what you can do - join us.

MAIN DUTIES AND RESPONSIBILITIES

Reporting to the Medical Area Lead, you will ensure planning and realization of research scientific projects for the assigned products according to corporate and local policies. You will provide high quality scientific support to Company functions (e.g. marketing, sales, regulatory, training, market access) and ensure planning and support to the Clinical Research Unit for the realization of clinical trials and for the assigned products.

**The role broadly includes the following key components**:
1. Ensure planning and realization of research projects for the assigned products according to corporate and local policies
2. Contribute, in co-operation with other Company’s functions, to the definition of the Product Business Plan (PBP) for the assigned products, according to the HQ strategies and policies
3. Prepare National Medical Plan on assigned product, providing strategies and objectives, according to the HQ strategies and policies
4. Collaborate with medical field team (MSLs and MSLs Manager), training them on product and disease update and supporting them in development of local medical plan
5. Ensure the Italian participation to the international clinical development (e.g.: by maintaining close contacts with the relevant international Product Teams)
6. Guarantee, with the Clinical Research Manager (CRM), the local implementation of global trials, according to planned milestones and costs
7. For local studies, review study proposals/protocols, ensure correct data management and analysis, ensure timely final study reports and publication of data
8. Provide high quality support to the Regulatory Affairs Dept in the definition and review of the product registration dossier and other documents, in compliance with HQ guidelines and MoH requirements
9. Provide support to Marketing Dept to guarantee the high quality scientific standard in the relevant activities [e.g: preparation and review of promotional material; planning and organisation of scientific events (e.g. symposia and/or lectures during congresses, updating course for medical targets, etc.)]
10. Provide support to Training Dept to guarantee that the Field Force receive high quality and updated scientific information on the products assigned
11. Support the Field Force in its relationship with medical target groups through continuous updating on therapeutic aspects related to the relevant pathology and/or products
12. Develop and maintain contacts with key Opinion Leaders and Scientific Community
13. Collect and discuss with sponsors the proposals for ESRs and to collaborate with the MEOR manager according to AZ SOP
14. Support the Medical Evidence and Observational Research (MEOR) Manager in the operational activities
15. Manage medical information requests
16. Manage budget
17. Manage all activities and Account relationship according with Company Values, Code of Conduct, Guidelines/Internal procedures and Italian legislation.

ESSENTIAL REQUIREMENTS

1. Medical Degree, preferably clinical experience in Amyloid Disease (cardiology, internal medicine setting)
2. Understanding of sales and marketing and pharmaceutical medical information
3. Knowledge of legislation relevant to pharmaceutical sales and marketing
4. Ability to manage incoming data and/or requests in a timely manner and escalate when appropriate

1. Proficiency in English and Italian

DESIRABLE REQUIREMENTS
1. PhD in the relevant Therapeutic Area
2. Experience in a pharmaceutical industry and Medical Affairs