Lieu de travail
Télétravail
Secteur d'activité
Industries
Date d'expiration
09 juillet
Niveau de poste
Manager / Responsable Département
Nombre de postes
1 poste ouvert
Type de contrat
CDI
Niveau d'étude (diplome)
Baccalauréat
Job Title: Medical Affairs Manager ALGERIA
About ANABION
We are ANABION, an international biotech company dedicated to helping people live longer and healthier lives. Our strong portfolio spans effective, safe, and affordable solutions in Life Sciences, including innovative treatments, biosimilars, and gene therapies for oncology, autoimmune disorders, and rare diseases such as SMA and hemophilia.
Key products and disease areas
· Biosimilars in oncology: pembrolizumab, bevacizumab, trastuzumab, rituximab
· Biosimilars in autoimmune, supportive care and rare diseases: eculizumab, darbepoetin alfa, adalimumab
· Original products in oncology: prolgolimab (anti-PD-1)
· Original products in autoimmune diseases: netakimab, levilimab (RA, PsA, Pso, Axial SpA)
· Original products in multiple sclerosis: divozilimab (anti-CD-20), sampeginterferon β-1a
Job Overview
We are looking for an experienced Medical Manager or Medical Advisor with knowledge across several disease areas, with a strong focus on oncology. The candidate should have a proven track record in product launches and a solid understanding of the different stages of clinical development.
Strong understanding of the multiple indications of pembrolizumab is very important, or the ability to quickly gain this expertise. The candidate should be able to independently organize and manage RWE studies and diagnostic programs, and lead these projects from concept and planning to execution and final results.
The role requires regular interaction with local authorities, KOLs, and partners, therefore strong communication skills are essential.
Key Responsibilities
Medical strategy development
Collaborate with cross-functional teams to develop and implement local medical strategies aligned with organizational goals.
Provide medical input into product development, clinical trials, and regulatory affairs.
Medical information and education
Act as a key source of medical knowledge for internal teams, external stakeholders, and customers.
Develop and deliver medical education and training programs for sales teams, healthcare professionals, and other relevant groups.
Regulatory compliance
Stay current with industry regulations and guidelines, ensuring that all medical activities adhere to legal and ethical standards.
Collaborate with regulatory affairs teams to support the preparation and submission of regulatory documents.
Key Opinion Leader (KOL) engagement and management
Build and maintain relationships with key opinion leaders, healthcare professionals, and experts in relevant medical fields.
Represent the organization at medical conferences, symposia, and other scientific forums.
RWE data generation
Design and coordinate real‑world evidence studies to support medical strategy, product positioning, and lifecycle management.
Collect, analyze, and interpret real‑world data (RWD) from healthcare providers, patient registries, and other external sources to generate actionable medical insights.
Qualifications
Background:
Medical degree (MD) or PhD in life sciences (i.e. cancer biology, molecular biology, or biochemistry,)
Industry Experience:
Previous experience in a similar medical management/advisory role within the healthcare or pharmaceutical industry.
Regulatory Knowledge:
Understanding of regulatory requirements and compliance in the healthcare and pharmaceutical sectors.
Analytical Skills:
Ability to critically analyze and interpret clinical data and scientific literature.
Understand concepts and terminology in biostatistics.
Team Collaboration:
Capacity to work collaboratively in cross-functional teams and communicate effectively with diverse stakeholders.
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