Hands on knowledge of good documentation practices
The role involves acting as the primary site contact and manager throughout all phases of a clinical research study
Job Summary
The role involves acting as the primary site contact and manager throughout all phases of a clinical research study.
Candidates must ensure data accuracy, subject safety, and protocol adherence while conducting remote and on-site monitoring.
The position requires collaboration with various functional areas including finance, regulatory affairs, and pharmacovigilance to support assigned sites.
Matching Summary
The role involves acting as the primary site contact and manager throughout all phases of a clinical research study.
Skills & Requirements
Must-have
Fluent in Local Languages and English
Good understanding of ICH-GCP guidelines
Hands on knowledge of Good Documentation Practices
Ability to perform root cause analysis
Experience with CTMS and eTMF systems
Nice-to-have
Developing ability to present technical information
Positive mindset and growth mindset
Ability to work independently and self-driven
Culturally sensitive working relationships
Solution-oriented approach to complex issues
Key Requirements
Associate's degree plus 3 years healthcare experience OR Bachelor's degree plus 6 months experience
Bachelor's degree in non-scientific field plus 2 years healthcare experience