On behalf of our Client a global pharmaceutical company, IQVIA is looking for aDeveloping Medical Expertwho can join an exciting working environment in a dynamic atmosphere areas in the therapeutic area ofoncology.
WORKING AREA:
South Italy
Residence: Sicilia
MAIN TASKS AND RESPONSABILITIES:
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 Company and the general medical communityCo-create medical multichannel campaigns, including content development, multichannel strategy and the customer journeyPlan and manage of 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 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 with latest scientific research on therapeutic area and competitors also attending appropriate national and international meetings and congressesDefine the strategic perspective and strong understanding of 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 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 withBe the central point of contact for any content related discussion 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, of 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 DegreePreferable 3+ years of professional experience in the medical/pharmaceutical field as a Medical/Scientific Advisor or Medical Science Liaison or in other Medical Department’s 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 digital approachAbility to perform successfully in a fast-paced, dynamic, team-based environment Willingness 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