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Medical Science Liaison

Il y a 2 mois

Paris, Île-de-France CSL Temps plein
About the Role

CSL Vifor is seeking a Medical Science Liaison to join our team in the West Region, covering the territories of Brittany, Centre-Loire, and Nouvelle-Aquitaine. As a Medical Science Liaison, you will be responsible for generating high-value regional medical projects, leveraging your expertise in nephrology (MRC and dialysis) and key opinion leaders (KOLs).

Key Responsibilities
  • Work closely with Regional Access to Markets (RAM) managers, Hospital Delegates (DH), and Zone Directors (DZ) to support regional and national strategy.
  • Collaborate with the Marketing Department at our headquarters.
  • Report to the Director of Medical Operations, who oversees a team of 4 Medical Science Liaisons.
Key Activities
  • Partnerships:
    • Establish high-quality scientific relationships with the medical community, including hospital chiefs, opinion leaders, and other recognized scientific influencers.
    • Build effective partnerships with external partners, including institutions and patient associations.
    • Organize and facilitate scientific meetings with KOLs (boards, conferences, round tables, etc.) to support the medical strategy of CSL Vifor products.
    • Provide medical counsel and assistance to Hospital Delegates, within the scope of valid AMM.
  • Medical Communication/Information:
    • Respond to healthcare professionals' requests.
    • Contribute to medical and scientific information on pivotal studies and product development, both internally and externally.
    • Provide accurate and relevant medical responses, backed by bibliographic research.
    • Ensure that the Medical Department receives a synthesis of valuable medical communications during conferences.
    • Keep up-to-date with scientific knowledge on products and update bibliographic information on product indications, based on field-collected information.
    • Participate in updating communication materials used by field medical teams.
    • Provide scientific support to Hospital Delegates, without interfering with their promotional role.
  • Development Clinical Studies and CSL Vifor Support (Phase IIIb and IV clinical studies, observational studies, IIS):
    • Propose relevant clinical studies.
    • Identify potential services that could play a key role in the conduct of clinical studies.
    • Set up and oversee the conduct of clinical studies, after validation of the protocol; supervise the follow-up of studies with the involved CRO.
  • Pharmacovigilance:
    • Transmit adverse event notifications to the Pharmacovigilance Department.
Requirements
  • Pharmacist, Medical Doctor, or PhD degree, or equivalent scientific background (BAC + 5 minimum).
  • 3-5 years of experience in the pharmaceutical industry, with expertise in interpreting, presenting, and/or following up on studies.
  • Specific knowledge: French regulatory framework (BPC, Pharmacovigilance, medical advertising, clinical study methodology). Ability to synthesize bibliographic articles.
  • Computer skills: excellent mastery of Word, Excel, and PowerPoint (for medical communication materials).
  • Fluent English (spoken, written, and read).