Write and review clinical (and nonclinical) documents for regulatory submissions in the EU and US, such as Module 2.5, 2.7, 2.4, 2.6, integrated summaries of efficacy/safety...
The role will provide leadership and strategic direction for assigned programs, ensuring the successful implementation of the quality strategy and/or quality plans to foster a...
Designs and delivers innovative & collaborative medical affairs projects, has a significant role in developing and driving the Medical Affairs Plan, operates as a medical reviewer...