Medical Science Liaison Italy

8 mesi fa

Milano, Italia TFS HealthScience A tempo pieno

Overview:
TFS HealthScience is excited to be expanding our SRS team and we are looking for an experienced, highly motivated Medical Science Liaison (MSL) in Italy who shares our vision of providing clinical research excellence. Our** **SRS team is a highly experienced international group of professionals led by an industry expert.

We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver.

Our cores values of Trust, Quality, Flexibility, Passion and Sustainability are what makes TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organisation.

**Together we make a difference.**

TFS HealthScience is looking for a Medical Science Liaison (MSL) hybrid based in Milan (Italy).

**What can we offer you?**

A great place to work where you will get the chance to push your career to the next level, global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients.

**Benefits include**:
Health Insurance

Lunch allowance

Home allowance

Possibility to compensate overtime

Flexibility

**Responsibilities**:
**General Mission**:
As the medical department's regional, national or international point of reference, the MSL's mission is to provide scientific and medical information in response to requests from healthcare professionals, and to develop scientific partnerships aimed at optimizing patient care and developing clinical research.

**Main Responsibilities**:
Regional medical strategy and project management:

- Identification of medical experts and institutional networks (healthcare decision-makers, public health organizations, etc.) in your area of expertise.
- Analysis of all the environmental characteristics of the therapeutic area in relation to the regional, national or international context
- Definition of strategic regional medical issues in line with corporate strategy
- Implementation and monitoring of regional medical plans
- Ensuring the scientific and ethical quality of projects
- Set up non-promotional regional medical operations with the region's expert healthcare professionals
- Set up programs to optimize patient care (care networks, information programs, observatories, etc.).
- Participate in or lead expert groups and round tables

Scientific and medical information for regional healthcare professionals:

- Share scientific and medical information (clinical and development data, publications, etc.) according to the needs of experts or healthcare professionals, through individual interviews or scientific meetings.
- Drafting of scientific information materials
- Answering scientific and medical questions, as required, on hospital medical committees responsible for the proper use of medicines.

Scientific and medical project management:

- Drawing up, implementing and monitoring regional medical plans (in line with national medical plans)
- Setting up and monitoring partnerships / scientific actions in line with the strategy established for the referent accounts
- Participation in medical congresses and sharing of information received

Help coordinate regional clinical operations:

- Identification and selection of scientific study projects proposed by clinicians in the region
- Participation in setting up and monitoring clinical studies conducted by the laboratory, in support of head office teams and clinical operations
- Presentation of preliminary study results

In-house information / consulting:

- Participation in skills development initiatives for the drug information and promotion network in its areas of expertise.
- Cross-functional information sharing, ensuring the reliability of information transcribed into reporting tools.
- Transmission of adverse event reports to the pharmacovigilance department.

Compliance with professional ethics:

- Relations with healthcare professionals based on the exchange of validated, high-quality information that is solely scientific and non-promotional.
- Sharing of skills needed to improve the use of the drug or its development
- Compliance of data delivered to healthcare professionals: up-to-date, scientifically-validated data and participation in the fight against scientific fraud
- Respect for the principles of data completeness and transparency: communication of all known and relevant data, whether positive or negative
- Critical analysis of data, study design, methodologies, analysis and/or presentation of results
- Following procedures when

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