Shreeya Patel is recruiting a Director, CMC, Regulatory Affairs to join a global pharmaceutical company in Hertfordshire.
As Director, CMC, Regulatory Affairs you will lead the Regulatory Affairs CMC UK team with the responsibility of growing the business, delivering excellent regulatory CMC services, maintaining and managing expert staff and contributing to the company's success worldwide. As Director, CMC, Regulatory you will be accountable for successful execution of multiple projects and stakeholders satisfaction. You will also provide leadership and direction to associate directors, managers and consulting employees.
As Director, CMC, Regulatory Affairs you will be involved in the management of all CMC projects, you will have experience of global regulatory filing and you will have experience of module 3 variations. Development experience is a must for this role as is the need for the Director, CMC, Regulatory Affairs to be involved in project work.
The main responsibilities for the Director, CMC, Regulatory Affairs include, but are not limited to, program oversight - ensuring quality of deliverables and services for multiple projects and products and staff management - recruiting and maintaining high-performing technical and management staff to execute projects and regulatory activity.
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL24389 in all correspondence. eMedCareers.com - 11 months ago
