- 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.
We currently have an opportunity for exceptional Regulatory Program Manager to join our global team. ...
- PW 6020 Regulatory Program Manager
Our client, a top global pharma company is looking for talented regulatory affairs professional. This role will be based at their award winning Development site and take responsibility for regional (EU, ROW) regulatory strategic and operational management of a project or portfolio of projects within their Oncology team.
- 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?
- Senior Clinical Supply Program Manager
We propose a permanent employment for a Senior Clinical Supply Program Manager. This pharmaceutical company is based in Brabant Wallon and very easily reachable. Job description This Clinical Supply Program manager will have the accountability at program level (for assigned programs). He will be a visible partner for Clinical development representatives, actively driving trial /packaging design and supply chain optimization. ...
- Clinical and Regulatory Records Manager
Clinical and Regulatory Records Manager - Leading Biopharmaceutical group
- SAS Programmer / Epidemiology Manager, Greater London
A unique and exciting opportunity has become available for an experienced SAS Programmer / Epidemiology Manager to join a rapidly growing and successful global Pharmaceutical company located in Greater London.
- Clinical and Reguatory Records Manager
A leading biopharmaceutical company focused on the discovery, development and commercialization of innovative drugs for diseases with significant unmet medical needs, is currently looking for a Clinical and Regulatory Records Manager to join them permanently in Switzerland. ...
- **Senior Manager Quality Assurance & QP - Very Interesting and Exciting Global Biopharmaceutical Company!**
One of my clients, a very interesting and exciting Global Biopharmaceutical Company are actively seeking a Senior QA Professional to join their Quality Assurance team in a Senior Manager role. This professional must also be a Qualified Person. The main focus of the role will be within the QA division, where the professional will have Senior oversight responsibilities of the Audit function and also the support of the regulatory inspections program.
- Clinical Records Manager
Our client is a leading biopharmaceutical company with more than 30 operating affiliates worldwide and specialises in respiratory and orphan diseases. The Clinical Records Manager will work within the Global Drug Regulatory Affairs department, managing the paper records for Global Clinical Development with an emphasis on adherence to Good Clinical Practice (GCP).
- PV Strategy Manager/Sr Manager
The PV Strategy Leads are responsible for the development and implementation of a risk-based quality assurance strategy that covers all PV processes and activities performed by Pharma global functions, Affiliates, service providers and licensing partners. This role conducts risk assessment to deliver an audit program, provides strategic direction to audit operations, and provide actionable data to senior management based on analysis of compliance data and identification of trends. ...