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About the role
Key responsibilities & impact- Support the coordination of clinical trial activities
- Maintain study documentation and site records
- Manage data entry and updates in electronic systems
- Communicate with patients, investigators, and external partners
- Assist with study-related documentation and translations
- Support investigators and medical staff in daily site activities
Requirements
What you’ll need- Fluent English, written and spoken
- Strong computer literacy and MS Office skills
- Excellent organizational and communication skills
- Attention to detail and ability to meet deadlines
- Positive, proactive, and team-oriented attitude
- Interest in building a career in clinical research
- Please submit your CV in English
Benefits
Comp & perks- Competitive salary package
- Performance-based bonus
- Meal vouchers
- Additional health insurance
- Comprehensive training and onboarding
- Professional development opportunities
- Supportive and collaborative team environment
- Career growth within Pratia and Humaneva Group