Junior Clinical Associate

Responsibilities

• Collection of regulatory documents.
• Serve as the point of contact between Study Teams and Clinical Trial Start-up Country Associate.
• Involvement into submission strategy for EMEA Region.
• Global knowledge of Clinical Trials regulations, GCP and ICH Guidelines for clinical research.
• Understand and comply with procedures
• Populate Trial Master Files and libraries for future reference
• Provide feedback and shared learning for continuous improvement
• Additional local responsibilities may be required as needed/appropriate for the local geography and/or to cover regional differences.  

Education:

• Bachelor’s degree preferably in a scientific or health related field, relevant experience appreciated.

Language

• Fluency in English and is essential, other language appreciated.

Experience

• Applied knowledge of project management processes and skills
• Experience in clinical research/ Involvement in cross-functional clinical trials
• Appreciation of / experience in compliance-driven environment
• Effective communication and problem-solving skills and demonstrated ability to meet timelines.
• Self-management and organizational skills.
• Knowledge of Good Clinical Practice and understanding of the overall drug development process