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Job Description

Antal international is a leading Head Hunting company globally present with more than 130 offices within 35 countries. Operations Division is particularly focused on high-skilled technical, engineering & scientific profiles.

On behalf of a Multinational Pharma Company Antal is looking for: 

MSL Veneto - Cardiovascular Area

To be a therapeutic area CardioVascular scientific expert, responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered a trusted scientific counterpart and partner.
To maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis. Through activities in line with the Medical Affairs Plan, the MSL is jointly responsible for the realization of short-term and long-term company goals.


 Develop and execute an external stakeholder management plan in close collaboration and coordination with RBD structures.
 Communicate the value of company products, contribute to e.g. market access activities and formulary discussions
 Through scientific interactions, champion the medical value of our products fairly based on the risk-benefit profile of our drugs and contribute to the fostering of innovative approaches
 Represent the company to other therapeutic area stakeholders including professional associations and patient organisations in cooperation with other Medical functions
 Proactive and reactive communication of medical scientific data to Leading Specialists and broader external health-care related audiences:
 Communicate non-promotional general information about our company, including pipeline, research and development programs and other relevant information
 Respond to unsolicited scientific queries from customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents
 Use digital technologies and new media to support proactive and reactive communication
 Organization and participation in Medical Education activities: Identify/support/educate speakers
 Act as a reference point for Sales Representatives for any scientific query, in collaboration with Medical Information as appropriate
 Support and manage Medical Affairs clinical activities strategy, planning, design and execution (in close co-operation with HQ and CROs)
 Support the set up and follow up of registries and other non-interventional Medical Affairs studies.
 Propose investigators and sites for interventional and non-interventional Medical Affairs studies
 Manage field based medical projects
 Ensure a link between HQ, local Medical Dept. and KOLs
 Contribute the pre-launch and launch steps of new products providing scientific support
 Represent  at medical meetings, conferences, advisory boards, etc at key institutions, and in interactions with key opinion leaders.
 Supports medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy.
 Assists with the scientific review, development, approval, execution and communication of affiliate medical affairs sponsored or supported clinical research activities.
 Visit Key Accounts and Key Opinion Leaders to answer any medical/scientific questions concerning the molecule / product
 Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
 Ability to work independently.



Medical Doctorate (M.D.) degree or equivalent with relevant therapeutic specialty in an academic or hospital environment in Cardio vascular & Metabolic disorders area. Completion of residency and/or fellowship is oncology area is “highly” preferred.
 Minimum of 2-5 years of MSL and or Medical Affairs and/or research and development experience in the biotech/ pharmaceutical industry.
 Must have an in-depth understanding of MSLs role and process.
 Proven leadership skills in a cross-functional team environment.
 Ability to interact externally and internally to support the business strategy.
 Good knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
 Strong understanding of the pharmaceutical business.
 Must possess good oral and written English communication skills.


Please send cv and contact details to:

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Camilla Mereghetti
+39 02 80 60 601