Medical Science Liaison, Iberia. Oncology

hace 4 semanas


Madrid, España Recordati Group A tiempo completo

Recordati, established in 1926, is an international pharmaceutical group, listed on the Italian Stock Exchange (Reuters RECI.MI, Bloomberg REC IM, ISIN IT 0003828271), 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.

**Purpose of the role**

We are recruiting for an experienced MSL for our Oncology Franchise in Iberia. The MSL will provide customer-oriented activities, medical and scientific support for the drugs he/she is responsible for at RRD across Iberia, in accordance with local codes of practice in place.

The role involves developing 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).

The MSL will participate in the training of regional and national experts on the scientific data of drugs for which he/she is responsible at RRD, and will spend approximately 70% of their time on customer-facing activities during the year.

**Key responsibilities**
- 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 off-label 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 drop-outs 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 programmes
- 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 in-depth 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 field-based staff
- Support speaker meetings e.g. via developing speakers and delivering specific scientific content
- Deliver peer-to-peer 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.
- Enter activity in RRD's CRM tool acc



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