Medical Science Liaison - Centro Italia Lazio

Medical Science Liaison - Centro Italia
Roma
Lazio, Lazio

On behalf of our Client, a global pharmaceutical company, IQVIA is looking for a Developing Medical Expert who can join an exciting working environment in a dynamic atmosphere in the therapeutic area of oncology.

WORKING AREA: MAIN TASKS AND RESPONSABILITIES: Contribute to the localization of the global medical and brand strategy Collaborate to drive medical strategy by translating the local medical plan into implementable TL engagement strategies with cross-functional teams and identify synergies with the interests of Company and the general medical community Co-create medical multichannel campaigns, including content development, multichannel strategy and the customer journey Plan and manage medical budgets related to the specific product Lead and align evidence generation with medical and brand strategy Foster Medical Affairs relationships with National TLs and external stakeholder groups Generate TL insights on unmet medical needs, document and communicate them in a flat network of autonomous entrepreneurial cross-functional teams to create tactics and strategy Identify any overlapping interests and potential synergies between the external stakeholder groups and Company Report external stakeholder engagement activities in Veeva Medical CRM Empower and foster collaboration with clinical trial teams on subjects related to interventional clinical trials including feasibility & initiation visits Review and interpret analytics and relevant field insights to optimize and manage medical content and adapt the evidence generation plan (e. g.

in National Advisory Boards) Keep abreast with the latest scientific research on the therapeutic area and competitors also attending appropriate national and international meetings and congresses Define the strategic perspective and strong understanding of Company's commercial, go-to-market strategies and healthcare landscape Document and process Medical Information (MI) queries in alignment with MI handling procedures Scientifically review and approve all therapeutic area/product related materials, external communications and advising cross-functionally Ensure that Company medical activities are in line with relevant guidelines, regulations and legislations Provide scientific education and training to cross-functional partners on product data, therapeutic area knowledge, and local clinical operations and clinical development studies Provide scientific contributions to development and implementation of Company-organized national, regional and local medical programs and gather competitive intelligence, build networks and build new material to engage TLs with Be the central point of contact for any content related discussion with the respective global structures Maintain regular and frequent contact with global project leads to ensure local projects and initiatives are appropriately aligned Responsible, as CPH Medical Content Creator, for product modular content strategy Lead implementation of projects, symposia and important meetings to engage TLs Support Market, Innovation Access & Regulatory presentations of new information to hospital formularies and reimbursement decision makers Lead TA/product cross-functional projects WHO YOU ARE: Scientific Degree Preferably 3+ years of professional experience in the medical/pharmaceutical field as a Medical/Scientific Advisor or Medical Science Liaison or in other Medical Department roles Strong skills in managing stakeholders and experienced in building networks Proven analytical and organizational skills Business Acumen and strong ability to influence decisions Proficiency in presenting to large internal/external audiences on highly relevant topics that have a significant impact Excellent informatics skills and open to digital approaches Ability to perform successfully in a fast-paced, dynamic, team-based environment Willingness to travel in the North of Italy Excellent knowledge of English (both spoken and written) TYPE OF CONTRACT: Chemical Contract – Permanent Staff Leasing Company Car IQVIA reserves the right to evaluate candidates with domicile/residence and work experience/study with requirements responding to the open request.

Applications WITHOUT the requirements will NOT be fully taken into account.

Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16) to IQVIA and to transfer those data to IQVIA's Clients.

The research is urgent and is intended for candidates of both sexes (L. 903/77).

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