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You will work closely with internal and external stakeholders to generate and communicate scientific insights, support clinical research activities and build meaningful scientific engagement with healthcare professionals and key opinion leaders.
Provide high-quality and timely responses to medical and scientific enquiries in accordance with applicable standards, including the development of standard response documents for frequently asked questions where appropriate.
Provide medical and scientific input into the development and execution of clinical trial and clinical research activities.
Support the initiation and oversight of clinical studies and research activities within the therapeutic area.
Build and maintain high-quality scientific dialogue with Key Opinion Leaders (KOLs), healthcare professionals and relevant external stakeholders.
Ensure medical materials provided by global or regional teams are appropriately tailored to local stakeholder needs and reviewed and approved according to applicable guidelines.
Generate and communicate relevant medical insights to cross-functional partners, including Pharmacovigilance, Regulatory Affairs, Market Access, Quality Assurance, Commercial and Brand teams.
Identify and assess risks within the area of responsibility, develop appropriate mitigation plans and support the implementation and monitoring of internal controls.
What You’ll Bring to the RoleEssential RequirementsRelevant scientific, medical or healthcare educational background.
Experience engaging with healthcare professionals and other scientific stakeholders.
Strong cross-functional collaboration skills and the ability to work effectively with Medical, Regulatory, Pharmacovigilance, Market Access, Quality and Commercial colleagues.
Strong communication and stakeholder-management capabilities.
Experience supporting clinical studies, Non-Interventional Studies or Investigator-Initiated Trials.
Key Measures of SuccessHigh-quality and timely delivery of Medical Affairs activities.
Quality and impact of medical and scientific stakeholder engagement.
Benefits & Rewards At Novartis, we’re committed to reimagining medicine together
- In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs.
In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines. Read our brochure to learn more about our global total rewards offering: Skills DesiredClinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Medical Information, Patient Care, Stakeholder EngagementSummaryLocation: Barcelona Gran Vía; Madrid DelegaciónType: Full time
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