Medical Advisor Cardiovascular

3 settimane fa

Milano, Italia AstraZeneca A tempo pieno

**Medical Advisor** **Cardiovascular**

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.

As **Medical Advisor Cardiovascular** you will contribute to the development of medical strategy and provide Medical input into Brand Strategies ensuring support of the life cycle of the assigned product.

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 Therapeutic Area Lead Cardiovascular, you will ensure planning and realization of research 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:

- Ensure planning and realization of research projects for the assigned products according to corporate and local policies
- 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
- Prepare National Medical Plan on assigned product, providing strategies and objectives, according to the HQ strategies and policies
- 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
- Ensure the Italian participation to the international clinical development (e.g.: by maintaining close contacts with the relevant international Product Teams)
- Guarantee, with the Clinical Research Manager (CRM), the local implementation of global trials, according to planned milestones and costs
- For local studies, review study proposals/protocols, ensure correct data management and analysis, ensure timely final study reports and publication of data
- 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
- 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.)]
- Provide support to Training Dept to guarantee that the Field Force receive high quality and updated scientific information on the products assigned
- 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
- Develop and maintain contacts with key External Expert and Scientific Community
- Collect and discuss with sponsors the proposals for ESRs and to collaborate with the MEOR manager according to AZ SOP
- Support the Medical Evidence Observational Research (MEOR) manager in the operational activities
- Manage medical information requests
- Manage all activities and Account relationship according with Company Values, Code of Conduct, Guidelines/Internal procedures and Italian legislation.

**ESSENTIAL REQUIREMENTS**
- Medical Degree (higly preferred) or Scientific degree
- Understanding of sales and marketing and pharmaceutical medical information
- Fundamental knowledge of basic research, drug development, clinical environment
- Detailed knowledge of the local regulatory requirements related to medical affairs activities
- Previous experience as MSL or Medical Advisor or other activities within the Medical Department roles
- Communication skills, including communicating detailed technical, scientific, or medical information
- Ability to work in team
- Leadership capabilities and interpersonal skills
- Project management experience
- Proficiency in written/spoken English and Italian
- Domicile in Lombardia

**Why AstraZeneca?**

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. We’re opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be.

The recruitment team will evaluate your profile and review your CV to determine whether your skills and exp

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