MSL (m/f/d)

MSL (M/F/D)

Tasks:

• Field-based consultant supporting the company with its Phase 3 clinical trials in the EU and UK.  Primary tasks include the following:
  • Recruitment of sites to participate in trial, site engagement, site initiation visits 
  • Advise regarding Protocol Design
  • Facilitate discussions between sites, principal investigators, supplement injection monitors / Rescue Monitors and company personnel in the United States
  • Provide scientific guidance at key regional and national congresses and, potentially provide medical booth support
  • Adhere to all company policies and standard procedures 
  • Comply with all statutory, regulatory and similar legislative requirements applicable to the provision of  tasks

Qualification:

• Successful track record as MSL in the Pharmaceutical Industry
• Expertise in Clinical Trial Management on a global scale
• Preferably Ophthalmology experience
• Existing network in either France or Italy
• Fluent in English and either French or Italian
• Excellent communication, stakeholder management and organization skills
• Flexible with time zones (mainly CET and EST)

Requirements: 

Start: April 2025

Duration: 12 months

Capacity: 5 days per week

Location: Italy or France - Remote and onsite at study sites