Clinical Study Delivery Specialist
hace 1 día
We are seeking a highly skilled Clinical Study Delivery Specialist to join our team. As a key member of our clinical operations team, you will play a critical role in ensuring the successful delivery of clinical trials.
Key Responsibilities- Provide support to the clinical trial team at the global level, impacting the project's success.
- Manage study trackers and access, ensuring timely distribution of dashboards and reports to the study team.
- System related support, including managing study systems, TMF management and maintenance, and providing timely follow-up with stakeholders to improve TMF compliance.
- Support common email groups for CSAP and CTMS issues, as well as clinical admin support and archival support.
- Excellent technical/IT skills, with the ability to understand the impact of technology on studies and use and develop computer skills.
- Knowledge of ICH GCP relevant operational procedures, systems, and quality guidelines.
- Able to work independently as well as in a team, with a professional attitude and good customer focus.
- Time management skills, with the ability to prioritize tasks and meet deadlines.
- Very good communication skills, with a high English level.
We offer a competitive salary, various annual leave entitlements, a range of health insurance offerings, and a Global Employee Assistance Programme. We are committed to providing an inclusive and accessible environment for all candidates and employees.
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. We are proud of our diverse workforce and the work we've done to become a more inclusive organisation.
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