- EU Principal Regulatory Program Manager anti-CD20, Hematology Franchise
The EU Principal Regulatory Program Manager on the anti-CD20 Team in the Hematology Franchise will play a key role in leading activities within the anti-CD20 regulatory team which includes the Gazyva/Gazyvaro and MabThera/Rituxan oncology projects in the Hematology Franchise. Such activities will include filings, regulatory maintenance activities and support for the medical affairs program. ...
- Principal Regulatory Program Manager
Reports to: Team Leader/ Senior GRL
The Principal Regulatory Program Manager is responsible for regional regulatory strategic and operational management of a complex project or portfolio of complex projects. Within this role, you will provide regional line management to regulatory partners working on the same projects.
Using your excellent communication skills, you will represent the regional function on cross-functional teams (e.g. ...
- EU Regulatory Affairs Program Manager
The program manager position will cover pediatric and adult programs in hematological malignancies and be responsible for the regulatory strategic and operational management. The role will report to the regulatory iPODD (innovative Pediatric Oncology Drug Development) franchise head. ...
- Regulatory Affairs Program Manager / Senior Regulatory Affairs Program Manager – Oncology
Regulatory Affairs Program Manager / Senior Regulatory Affairs Program Manager – Oncology
Are you looking to work for a major Pharmaceutical organisation that embraces innovation with an exciting product portfolio?
Do you want to work for one of the most reputable and respected businesses in the pharmaceutical industry?
Are you looking for structured career progression, both financially and professionally?
- Contract Clinical Program Manager
A leading global pharmaceutical company has a new vacancy for a Contract Clinical Program Manager to join their expanding Central London team. The company has a superb pipeline and operates in over 90 countries around the world. This is a 6 month contract role with the possibility of an extension. ...
- Regulatory Lifecycle Manager EU or GLOBAL ** Blockbuster management post licencing / Belgium
****Regulatory Lifecycle Manager EU or GLOBAL ****
Please call one of Advanced Regulatory’s Principals for Regulatory Affairs, Theo Moore on +44 (0)207 801 3384 or +44 (0)7918 195 166. Alternatively you can email me on Theo@AdvRegulatory.com
- Clinical Program Manager
This job is a great opportunity for a Clinical Program Manager to work at one of the top 10 global pharmaceutical companies. This role will be based at the company’s West London office with some flexible home working. The organisation develops innovative products across multiple therapy areas including cardiovascular, oncology, and respiratory, and employs 100,000 staff globally. This is a 6 month contract role with the possibility of an extension. ...
- European Director Program Management (Based out of UK)
This is a newly created position within my growing pharmaceutical client. Morgan Prestwich has been retained to find a European Director Program Management. The position has multidisciplinary responsibility for the impending launch of a new product to market. The Director Program Management for Europe, will work closely with their Global teams, but have overall responsibility for Europe.
- Clinical Manager Medical Devices
Clinical Manager Medical Devices
Employment Type: Permanent, Office-Based
Salary: Up to 85,000€/gross/year plus benefits
- Director Program Management
This is a newly created position within my growing pharmaceutical client. Morgan Prestwich has been retained to find a Director Program Management to be based on East Coast USA. The position has multidisciplinary responsibility for the impending launch of a new product to market. The Director Program Management will work with their Global teams.