Development Medical Expert (Sud Italia) at IQVIA
Palermo, Sicilia, Italy -
Full Time


Start Date

Immediate

Expiry Date

05 Jul, 25

Salary

0.0

Posted On

30 May, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

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 areas in the therapeutic area of oncology.

Responsibilities
  • 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 of 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 latest scientific research on 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, of 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
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