Job Overview:
The Sub-Investigator plays a pivotal role in the success of clinical research studies by ensuring compliance with established protocols, conducting thorough assessments, and maintaining participant safety.
Main Responsibilities:
* Data collection and analysis
* Effective management of investigational products
* Collaboration with the site team to ensure seamless project execution
* Maintenance of regulatory documentation and adherence to industry standards
* Engagement and communication with participants
Essential Skills and Qualifications:
* Clinical expertise, including patient assessment, data collection, and participant safety monitoring
* Familiarity with regulatory requirements and experience in compliance with clinical trial protocols and documentation standards
* Excellent communication and teamwork abilities to facilitate collaboration with researchers, participants, and the clinical team
* A high degree of attention to detail and analytical skills for accurate data review and investigational product management
* Prior experience in clinical research or related medical roles is highly desirable