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Medical Manager, Rare Diseases - Hematology & Nephrology

astrazeneca

New
Mid 🇬🇧 English
Real-world evidence (RWE) Clinical research Pharmacovigilance Medical affairs

Job description

About the role

AstraZeneca is looking for a Medical Manager for its Rare Diseases portfolio covering Hematology and Nephrology. The role drives medically led initiatives, leads real-world evidence (RWE) projects and shapes the scientific and patient-facing approach to rare diseases, working with Medical Affairs and cross-functional teams.

Key responsibilities

  • Drive medically led initiatives with cross-functional teams to improve patient outcomes in Hematology and Nephrology rare diseases.
  • Design, implement and lead RWE projects, interpret their findings and use them to inform medical and commercial strategy.
  • Lead educational initiatives and develop clinical support tools to close gaps in disease awareness, diagnosis, referral pathways and patient management.
  • Align the Field Medical Strategic Plan and MSL activities with Medical Affairs plans and portfolio priorities, using data-driven decisions and digital tools.
  • Ensure product materials are scientifically accurate, hold signatory authority on therapy area materials and advise marketing teams on medical accuracy.
  • Oversee governance and compliance, including clinical trials, promotional activity, patient safety and pharmacovigilance.

Required profile

  • Bachelor's degree in Medicine, Pharmacy or a relevant Life Sciences discipline.
  • 2 years of relevant experience in Medical Affairs or a scientific/clinical role in a multinational pharmaceutical company.
  • Fluent written and spoken English.
  • Desirable: previous experience in Rare Diseases, Hematology and/or Nephrology, and experience in Medical Affairs or field medical roles.

Required skills

  • Strong medical and scientific knowledge and the ability to interpret and communicate complex clinical data.
  • Ability to develop and execute medical strategies and engage with healthcare professionals and external stakeholders.
  • Sound understanding of pharmaceutical governance, compliance and ethical standards.
  • Desirable: experience in evidence generation (RWE and/or clinical research), project management and new product launch preparation.

Questions fréquentes

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Source : ats:workday

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Published 10 hours ago

Expires 1 month from now

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