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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
- Recruitment of sites to participate in trial, site engagement, site initiation visits
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
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