- 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. ...
- Senior Regulatory Program Manager
The Program Manager position will be responsible for regional (EU, ROW) regulatory strategic and operational management of a project, , or a portfolio of projects
Primary Responsibilities and Accountabilities
Is responsible for and leads the development and implementation of regional regulatory strategies on projects
Gives regional strategic regulatory input to the RAFT and Project Teams for lifecycle management of products
Analyzes regulatory environment for impact on project/p ...
- Regulatory Program Manager - Immunology
We currently have an opportunity for exceptional Regulatory Programme Managers to join our global team working specifically on our Immunology portfolio. You will be responsible for Phase II / III projects, ultimately resulting in MAA preparation and filing. This role can be based in Welwyn Garden City in the UK or Basel in Switzerland. ...
- Associate / Regulatory Program Manager
Roche are at the forefront of developing ground-breaking new medicines and consistently push the boundaries of conventional thinking and embrace innovation across our business. With a strong pipeline, we are looking for people to support global teams to develop and gain approvals for medicines in Europe and Rest of World countries. ...
- 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
- 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.
- Senior Regulatory Affairs Manager (Associate Director Level) North Carolina - USA
An Excellent opportunity have arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company within the US - North Carolina - OFFICE based in the RTP - PERMANENT postion.
- **GCP Quality Assurance Manager - Brussels, Belgium**
I am exclusively representing one of the biggest industry names in their search for a GCP Quality Manager based close to Brussels. This role will be placed within the Global GCP Audit and Inspections program, and requires a professional with a strong Clinical background, Auditing expertise, and a true Solution Orientated mind set. The company can offer a fantastic salary along with a very strong benefits package, guaranteed bonus and stock options.
- Senior Strategist
Working as part of the Genpact Pharmalink Consulting team gives you a career that will be varied, diverse and never dull! You will be joining a team of the best Regulatory Affairs Professionals in the industry, some of the most experienced and progressive minds. Our consultants come from a wide spectrum within the Healthcare Industry, all bringing invaluable skills and attributes that allow us to provide the best Regulatory Affairs expertise to our clients.
- Marketing - EMEA Biosimilars New Product Launch Manager
The EMEA New Product Launch Manager for the Commercial Biosimilars platform has overall accountability for managing and overseeing the cross-functional activities required to ensure the timely launch of new biosimilar products in the EMEA marketplace.