Clinical Data Entry/study Coordinator

hace 2 días


Sevilla, España TFS A tiempo completo

Key Responsibilities
- Data Entry
- Queries resolution
- Assist with SAE notification
- Help investigator with patient recruitment
- Facilitate Ethics Committee submissions
- Attend Monitoring visits
- Investigator File updating
- Patient visits schedule
- Study Drug Accountability and Dispensing logs
- Sample shipment
- Patients expenses payment
- Assist in investigators meetings or training when required

**Requirements**:
**Requirements**:
Bachelor’s Degree, preferably in life science
- Previous experience on clinical research, or Master related studies
- Excellent organizational skills and demonstrated ability to prioritize and handle multiple

competing priorities
- Adaptability and flexibility to changing priorities, with ability to maintain demanding timelines
- Good oral, written and communication skills in English
- Ability and willingness to travel

**Benefits**:
25 working days per year of service

Flexible working times
TFS Academy training courses
Free Private Health Insurance

Flexible remuneration scheme including Nursery ticket and Training


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