Hands on knowledge of good documentation practices
The role acts as the primary site contact and manager throughout all phases of a clinical research study
Job Summary
The role acts 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 performing 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 acts 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
Experience with CTMS and eTMF systems
Ability to perform root cause analysis
Nice-to-have
Strong interpersonal and conflict management skills
Solution-oriented approach to complex issues
Positive growth mindset and self-driven attitude
Ability to work in a matrix multicultural environment
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