Site Activation Professional
Há 3 horas
Job Overview:
This role involves performing site activation activities at a country level, associated with regulatory requirements, SOPs, and project guidelines.
Key Responsibilities:
- Execute site activation tasks in assigned studies for investigative sites, adhering to applicable regulations and work instructions.
- Review documents for completeness, accuracy, and consistency under senior staff guidance.
- Prepare site regulatory documents, ensuring completeness and accuracy.
- Notify team members of completed regulatory and contractual documents for individual sites.
- Distribute completed documents to sites and internal teams.
- Maintain accurate and complete project-specific information in internal systems, databases, and tracking tools.
- Track the progress, approval, and execution of documents, including regulatory, ethics, and Investigator Pack release documents.
Required Skills and Qualifications:
- High School Diploma or equivalent.
- 1 year' experience in regulatory and Start-up area.
- Strong interpersonal communication and organizational skills.
- Attention to detail.
- Familiarity with the clinical trial environment and drug development process.
- Ability to work on multiple projects.
- Effective working relationships with co-workers, managers, and sponsors.
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