Medical Science Liaison, Iberia - Madrid, España - Recordati Group

Recordati Group

Empresa verificada

Madrid, España

hace 3 semanas

Publicado por:

Isabel García

beBee Recruiter

Descripción

Recordati, established in 1926, is an international pharmaceutical group, listed on the Italian Stock Exchange (Reuters RECI.MI, Bloomberg REC IM, ISIN IT , with a total staff of more than 4,300, dedicated to the research, development, manufacturing and marketing of pharmaceuticals. Headquartered in Milan, Italy, Recordati has operations in Europe, Russia and the other C.I.S. countries, Ukraine, Turkey, North Africa, the United States of America, Canada, Mexico, some South American countries, Japan and Australia.

An efficient field force of medical representatives promotes a wide range of innovative pharmaceuticals, both proprietary and under license, in several therapeutic areas including a specialized business dedicated to treatments for rare diseases.

Recordati is a partner of choice for new product licenses for its territories. Recordati is committed to the research and development of new specialties with a focus on treatments for rare diseases.

Role Purpose

Based in Madrid, the MSL will provide customer-oriented activities, medical and scientific support for the drugs he/she is responsible for at Recordati Rare Diseases (RRD) in assigned territories across the Iberia region with local codes of practice in place.

The MSL will develop professional relationships with key customers to understand and improve the patient care journey (e.g. diagnosis, accessibility to treatment or diagnosis, disease awareness, understand epidemiology and facilitate the development of scientific programs) and participate in the training of regional and national experts on the scientific data of drugs for which he/she is responsible at RRD.

The Medical Science Liaison will spend approximately 70% of their time on customer-facing activities during the year.

Role Requirements

Ensure timely and informative scientific / medical exchanges with external customers and internal partners, which accurately reflect scientific data, in accordance with compliance policies and procedures as well as with legal and ethical standards
Ensure continuous medical education, clinical doubts resolution and responses to solicited requests of information
Be the local contact point with the patient's association or representative.
Deliver medical / scientific training to healthcare professionals on the scientific data of drugs for which he/she is responsible at RRD.
Be the products medical reference for the field force, the physicians and for HQ bringing medical expertise
Monitor with the Medical Department the needs of each Key Opinion Leader (KOL) or Hospital regarding scientific questions and support medical information in building these responses
Identify, build and maintain strong relationship with local opinion leaders, promote the publication of interesting case reports, encourage doctors to present Real World Evidence data in congresses and meetings and develop actions plans by territory with the KAM in line with the Brand plan
Develop opportunities to generate local data including poster, publication and speaker presentations
For requests concerning offlabel indications, collect requests for information and provide available information (bibliography or on the possible development of new indications) and monitor the management of these patients (pharmacovigilance)
Facilitate the organization of Advisory Boards and Scientific meeting related to the top priority brands
Treatment dropouts follow up: generate meetings with the doctors, obtain clinical information, design an action plan for restarting the treatment and bring medical evidence about the chronicity of the illnesses
Participate actively in the training programs
Provide scientific support for medical, marketing and market access activities as required (e.g. promotional copy design, brand claims, brand reviews, market research, advisory boards)
When applicable participate actively in documents preparation with an indepth material revision
When applicable provide medical approval and certification of local promotional materials and activities in accordance with the Code of Practice
Deliver quality medical education presentations in a variety of settings and obtain feedback that can be disseminated throughout the organization e.g. staff meetings, round tables, hospital meeting activities in collaboration with the commercial fieldbased staff
Support speaker meetings e.g. via developing speakers and delivering specific scientific content
Deliver peertopeer clinical and scientific communications to develop expertise of regional and national KOLs in assigned medicines
When needed attend and support at International, European and local congresses / symposia (if needed or required by the needs of the business).
Act as an ethical leader, work in team and demonstrate excellent awareness of the ethical, governance and compliance framework both internally and externally.
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