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Medical Science Liaison Cardiovascular (Lombardia e Sardegna)

Lieu Milan, Lombardie, Italie Job ID R-217568 Date de publication 01/17/2025

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. At AstraZeneca every one of our employees makes a difference to patient lives every day.

As Medical Science Liaison Cardiovascular (Lombardia e Sardegna) you will act as critical strategic regional contributor in initiating and implementing medical plan in support of AZ pipeline. You will be as the first point of contact for any medical/scientific aspect or issue related to the assigned products by engaging in Scientific Exchange with AstraZeneca teams, Key External Experts, Health Care Professionals, and Clinical Investigators.

At AstraZeneca, Cardiovascular, Renal and Metabolic (CVRM) is one of our main therapy areas because science continues to uncover commonalities between these diseases. With this knowledge, we are daring to do things differently by shifting focus from treating patients with a single disease, to addressing overlapping disease areas and risk factors. This new approach gives us the chance to save vital time and valuable healthcare resources, and most importantly improve patient lives.

MAIN DUTIES AND RESPONSIBILITIES

Reporting to the MSL Manager you will build and maintain strong scientific understanding of AZ marketed products, drive the identification f the unmet needs related to the development pipeline compounds and collect strategic insights.  You will leverage on strong scientific and clinical expertise to create and develop professional partnership with Key External Experts (KEEs) including new targets, relevant for the implementation of cardiovascular plan (basically cardioogists, neurologists, internal  medicine KEEs in a non-promotional scientific context as determined by global and local Medical Affairs plans.

The role broadly includes the following key components:

  • Closely strong cross-functional collaboration (with AM, ISF, RAM, LAM, MA, TAL, MKT ) to support business opportunity and strategic objective through regular contacts and team meetings;

  • Support the Field Force in its relationship with medical target groups through a continuous updating on therapeutic aspects related to the relevant pathology and/or products;

  • Provide medical input to Competitive Intelligence Department, including critical review of competitor data/scientific material;

  • Identify local medical needs and define a Local Scientific Plan (LSP), according to the Italian and HQ strategies and policies, to be integrated into the local business plan;

  • Provide input and support to Medical Advisors/Medical Lead and Clinical Operations Team in sites selection and feasibility assessment for national/international trials, and in the management of potential issues related to the implementation and conduct of international/national trials;

  • Evidence generation: identify evidence gaps, collect and discuss with Investigators the proposal for independent studies (ESR Externally Sponsored Research) in line with the CV strategic plan and, according to SOP;

  • Develop and maintain contacts with Scientific Societies/Communities;

  • Medical Education: manage medical information requests, continuously support activities aimed to disseminate science to KEEs in a compliant way, through face-to-face/online interaction and residential events

  • Manage all activities and Account relationship according to Company Values, Code of Conduct, Guidelines/Internal procedures and Italian legislation

  • Provide support to the Field Force to guarantee high quality scientific standards in the relevant activities (e.g: planning organization and participation at regional scientific events);

  • Support the Medical Advisers/Medical Lead and Patient Safety Department in the management of AEs (e.g collection of follow-up information)

ESSENTIAL REQUIREMENTS

  • Scientific Degree, scientific and clinical understanding

  • Fundamental knowledge of basic research, drug discovery, drug development, clinical environment

  • Knowledge of the local regulatory requirements related to medical affairs activities

  • Strong leadership capabilities

  • Empowerment and accountability

  • Excellent interpersonal skills

  • Project management experience

  • Communication skills, including communicating complex technical, scientific, or medical information

  • Ability to work in team

  • Networking and influencing skills

  • Understanding of written/spoken English

  • Willingness to be part of international teams

  • Domicile in the working area

DESIRABLE REQUIREMENTS

  • Knowledge of the Therapeutic Area

  • Experience as MSL or Medical Affairs

  • Medical Degree

  • PhD in the relevant TA

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.

Next Steps – Apply today!

To be considered for this exciting opportunity, please complete the full application.

The recruitment team will evaluate your profile and review your CV to determine whether your skills and experience match the job profile.

Only shortlisted candidates matching the job profile will be contacted for an interview. If you are recently being involved into a recruitment process for a similar professional role within our Company, we will evaluate our previous feedback to arrange an interview.

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law



AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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