Summary:
The role involves providing support for study coordination data management and regulatory activities within a Clinical Trials Office (CTO). This position ensures compliance with protocol guidelines internal procedures and regulatory requirements while assisting multidisciplinary teams in research activities.
Responsibilities:
- Ensure all study requirements are documented and comply with internal and external regulations following protocol guidelines.
- Maintain logs including tracker submissions and update the CTO OnCore database in a timely manner per CTO SOPs.
- Respond to queries promptly and accurately.
- Schedule and participate in monitoring visits.
- Attend multidisciplinary team program meetings as required.
- Assist multidisciplinary teams in various research activities.
Requirements
Requirements:
- Bachelor s degree or an equivalent combination of education and experience.
- Medical and/or science education or experience is preferred.
- Proficiency in Microsoft Office Suite including Excel and PowerPoint.
- Strong attention to detail and organizational skills.