Sr. Associate – Clinical Trial Start Up – Israeli / Hebrew
Eli Lilly
Key Responsibilities
- Initiate investigator site activities
- Collection and submission of regulatory documents
- Customize and negotiate informed consent documents
- Serve as point of contact for ERB and Competent Authority
- Communicate and negotiate budgets with site personnel
- Track and ensure site compliance to required training
- Communicate directly with sites for start-up and maintenance
- Identify, communicate, and resolve issues
- Ensure country specific regulatory and data privacy requirements compliance
- Populate internal systems for trial/site performance tracking
- Manage Trial Master Files and libraries
- Provide feedback for continuous improvement
Requirements
Education
Bachelor's degree in scientific or health related field
Experience
2 years clinical research experience preferred
Required Skills
- Native Hebrew/Israeli language proficiency
- Fluent English
- Project management
- Communication skills
- Negotiation skills
- Problem solving skills
- Self-management
- Organizational skills
- Understanding of clinical development paradigm
Benefits
- Gym membership
- On-site gym
- On-site parking
- Healthcare
- Pension
- Life assurance
- Subsidised canteen
- Travel subsidies
- Educational assistance
- Flexible hybrid working
- Wellbeing initiatives
Original Job Posting: View on Source Website