About the Client
Our client is a global biotech company developing cell-targeting therapies using an unique technology, with the goal to broaden the scope in cancer treatments.
The company provides great talent development opportunities for people who are eager to build a career in a fast-paced environment.

Role's Responsibilities
- Leader of 1-3 studies through clinical studies activities that meet ICH/GCP/SOP requirements.
- Manage clinical studies from planning to closure including goal-setting, timeline, and budget.
- Oversee the performance of study team members in either a matrix management model or as direct reports.
- Manage study-related vendors including CROs and contract labs.
- Responsible for ensuring development and implementation of applicable study plans, e.g., protocols/amendments, informed consent templates, Communication/Risk Mitigation Plan, eCRF & CRF forms/completion guidelines and site reference manu...