Core Responsibilities:
- Support Medical Monitors (MM) and Medical Affairs (MA) management in various tasks.
- Provide medical/scientific consultation with oversight from MM.
- Manage safety-related issues with investigational sites and clients.
- Assist with clinical data review, financial tracking, and maintaining project files.
- Contribute to internal/external deliverables such as trackers, reports, and presentations.
- Collaborate across departments (e.g., safety, regulatory) for updates on serious adverse events (SAEs) and regulatory concerns.
Qualifications:
- Degree: Health-related field.
- Experience: At least 2 years in clinical research or related industry.
- Skills:
- Proficiency in medical terminology and coding systems.
- Knowledge of ICH guidelines.
- Strong communication in advanced English (written and verbal).
- MS Office skills and experience in the pharma sector (desirable).
Benefits and Perks at ICON:
- Annual leave and flexible work arrangements.
- Comprehensive health insurance and retirement savings plans.
- Global Employee Assistance Programme (LifeWorks).
- Life assurance and other country-specific perks (gym memberships, subsidized travel, etc.).
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