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 under the support of senior CRAs
Job Summary
The role acts as the primary site contact and manager throughout all phases of a clinical research study under the support of senior CRAs.
Responsibilities include performing remote and on-site monitoring to ensure data accuracy, subject safety, and protocol adherence.
Candidates must possess strong communication skills to collaborate with investigators, vendors, and internal functional areas while managing regulatory documentation.
Matching Summary
The role acts as the primary site contact and manager throughout all phases of a clinical research study under the support of senior CRAs.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Fluent in local languages and English
Knowledge of ICH-GCP and local laws
Hands-on knowledge of Good Documentation Practices
Experience with CTMS and eTMF systems
Ability to perform root cause analysis
Nice-to-have
Solution-oriented approach to complex issues
High sense of accountability and urgency
Ability to work in multicultural matrix environment
Positive growth mindset
Strong interpersonal and conflict management skills
Key Requirements
Associate's degree plus 3 years healthcare experience OR Bachelor's degree plus 6 months healthcare experience
Bachelor's degree in non-scientific field plus 2 years healthcare experience