We're sorry, the job you are looking for at Moderna on EuroPharmaJobs has expired.
Click here to see more jobs at Moderna.
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
Develop and contribute to content, format and accountability for regulatory submissions and related supplements and amendments, regulatory documents such as meeting requests,...
Single point of contact/single point of accountability within GRA on the Core Asset Team (CTA) and Medicines Development Team (MDT) for assigned program(s); Chairs a Global...
Oversee all activities of Medical Writing staff including hiring; project assignments; training on policies and procedures; performance review and rewards; and budget and resource...
Ensure collaboration with the global regulatory team in preparing global regulatory strategies, identifying regulatory opportunities and mitigating risks, developing competitive...
This Senior Regulatory Affairs Manager will develop and lead the implementation of a robust control infrastructure and governance within Regulatory Affairs inclusive of processes,...
The Sr Director will provide regulatory support across the Therapeutic Areas including Infectious Diseases, Oncology, Cardiovascular and Rare diseases and, as a secondary role,...
Represent International region in Global Regulatory Teams and other cross-functional forums, for assigned development projects. Develop International regulatory strategies and...
The Head of Regulatory Affairs provides regulatory vision and leadership to the Affiliate. S/he executes these responsibilities by utilizing experience, knowledge of regulatory...
We are looking for a Regulatory Affairs Director to lead a team who thrives in a multifaceted environment, enjoys helping employees reach their potential, and encourages new...
In collaboration with project team members, defines project requirements and timelines. Organizes, creates, and maintains project plans, communicates project status to...
The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure. The...
Responsible for developing and executing the Clinical Development Plan (CDP) for ≥ 1 indication in an oncology development program at MorphoSys. Lead Medical Scientists and...
This position will provide leadership, planning, direction, communication and coaching to partner with the Process Owner for GxP regulated processes in the development and...
Provide support and guidance to other cross functional team members on various topics in countries with regulatory framework of lower complexity or higher with support of line...
Develop Europe regulatory strategy and provide regulatory expertise within project/product teams for products under development and/or marketed products as required. Lead and...