Your Tasks and Responsibilities
As a part of the Clinical Development Department, you will contribute to the successful execution of our clinical development plans for iOmx investigational products. You will work in an interdisciplinary team and will lead the outsourced activities for conducting clinical trials.
Some of your daily tasks will include:
Some of your daily tasks will include:
- Overseeing the planning and management of clinical trials, including selection and supervision of CROs.
- Contributing to clinical development plans and study protocols from the operations perspective.
- Acting as a key member of a cross-functional clinical development team (clinical operations, data management, safety reporting, etc.) to effectively plan and execute study activities aligned with the overall development strategy.
- Mentoring and developing assigned staff, as needed.
- Working with study sites and investigators to ensure efficient performance and completion of clinical studies.
- Supporting project budget planning and monitoring in collaboration with the Head of Clinical Development and the project leader.