As a Principal Clinical Data Scientist, you will lead the management of data for multiple studies.
Key Responsibilities
* Direct functional activities for medium to large projects in clinical studies, ensuring efficient execution of pharmaceutical drug development plans.
* Coordinate data management activities internally and externally, fostering collaboration and effective communication.
* Making informed decisions on data management strategies at study or project levels, driving compliance and efficiency.
This role offers an opportunity to develop expertise in end-to-end processes, from protocol development to reporting, with comprehensive training and support.
Requirements
* Relevant academic qualifications, such as a degree or Master's.
* At least 9 years' experience in Drug Development, with a minimum of 8 years in Clinical Data Management.
* Proven track record across multiple end-to-end studies, with a strong understanding of data management principles.
Advanced Opportunities Ahead: This position presents a unique chance to grow professionally, taking your skills and expertise to new heights.