Development Medical Expert (Sud Italia) PALERMO

Development Medical Expert (Sud Italia)
Palermo
Sicilia, PALERMO

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: South Italy

Residence: Sicilia

MAIN TASKS AND RESPONSIBILITIES: Contribute to the localization of the global medical and brand strategyCollaborate 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 the Company and the general medical communityCo-create medical multichannel campaigns, including content development, multichannel strategy, and the customer journeyPlan and manage medical budgets related to the specific productLead and align evidence generation with medical and brand strategyFoster Medical Affairs relationships with National TLs and external stakeholder groupsGenerate TL insights on unmet medical needs, document and communicate them in a flat network of autonomous entrepreneurial cross-functional teams to create tactics and strategyIdentify any overlapping interests and potential synergies between the external stakeholder groups and the CompanyReport external stakeholder engagement activities in Veeva Medical CRMEmpower and foster collaboration with clinical trial teams on subjects related to interventional clinical trials including feasibility & initiation visitsReview 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 of the latest scientific research on the therapeutic area and competitors by attending appropriate national and international meetings and congressesDefine the strategic perspective and strong understanding of the Company's commercial, go-to-market strategies, and healthcare landscapeDocument and process Medical Information (MI) queries in alignment with MI handling proceduresScientifically review and approve all therapeutic area/product related materials, external communications, and advising cross-functionallyEnsure that Company medical activities are in line with relevant guidelines, regulations, and legislationsProvide scientific education and training to cross-functional partners on product data, therapeutic area knowledge, and local clinical operations and clinical development studiesProvide scientific contributions to the development and implementation of Company-organized national, regional, and local medical programs and gather competitive intelligence, build networks, and create new materials to engage TLsBe the central point of contact for any content-related discussions with the respective global structuresMaintain regular and frequent contact with global project leads to ensure local projects and initiatives are appropriately alignedResponsible, as CPH Medical Content Creator, for product modular content strategyLead implementation of projects, symposia, and important meetings to engage TLsSupport Market, Innovation Access & Regulatory presentations of new information to hospital formularies and reimbursement decision-makersLead TA/product cross-functional projectsWHO YOU ARE: Scientific DegreePreferably 3+ years of professional experience in the medical/pharmaceutical field as a Medical/Scientific Advisor or Medical Science Liaison or in other Medical Department rolesStrong skills in managing stakeholders and experienced in building networksProven analytical and organizational skillsBusiness Acumen and strong ability to influence decisionsProficiency in presenting to large internal/external audiences on highly relevant topics that have a significant impactExcellent informatics skills and open to a digital approachAbility to perform successfully in a fast-paced, dynamic, team-based environmentWillingness to travel in the North of ItalyExcellent knowledge of English (both spoken and written)TYPE OF CONTRACT: Chemical Contract – Permanent Staff LeasingCompany CarSales Incentive PlanIQVIA 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).

#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs. iqvia.com

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