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Medical Lead

1 month ago


Copenhagen, Copenhagen, Denmark Novartis Full time

About the Role Your Key Responsibilities:
Your responsibilities include, but are not limited to:

  • Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, for frequently asked questions.
  • Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the respective therapeutic area.
  • Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities.
  • Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines.
  • Ensure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.
  • Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt - Distribution of marketing samples (where applicable).

Essential Requirements:

  • Min. 3 years of experience in Medical Affairs from the Pharma industry.
  • Education: Life Sciences Degree.
  • Proficient Danish and English, both written and spoken.
  • Project Management.
  • Stakeholder Engagement.

Commitment to Diversity and Inclusion / EEO:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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