Study Coordinator - Freelance / Contractor
TFS, France

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

• 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

Flexible working times

TFS Academy training courses

Free Private Health Insurance (CIGNA)

Flexible remuneration scheme including Nursery ticket and Training

Equipment and Internet costs covered by TFS

Job Rewards and Benefits