In this role you are accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, clients policies and procedures, quality standards and adverse event reporting requirements internally and externally. You would be responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.
With the support of exceptional people and an energized purpose, youll be empowered to own your career journey with dedicated mentoring, training and personalized development planning.
Requirements: - University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
Experience
- Good organizational and time management skills
- Working knowledge of ICH, FDA, local regulatory requirements, IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start up documents; previous interaction with operational project team and investigative sites preferred.
- Interact with internal and external customers with high degree of professionalism and discretion
- Good computer skills with good working knowledge of a range of computer packages
- Fluent English and Hebrew
This position is open to all candidates.
