- 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.
- Senior Regulatory Affairs Program Manager - Clinical Trial Applications
My client is a global pharmaceutical company, with offices across the globe.
- Principal Regulatory Consultant - Regulatory Affairs Project Manager
Principal Regulatory Consultant - Regulatory Affairs Project Manager
Up to £65,000 per annum plus benefits. This role is purely home based with no office working.
Having won numerous industry awards and acquired many businesses our client has taken the Pharmaceutical industry by storm. Our client has supported all of the top 20 leading biotechnology companies, all of the top 10 largest pharmaceutical companies and nearly all of the 50 best-selling drugs on the market right now.
- Program Manager
• Program Manager
• Niche pharmaceutical company
• Permanent role
• Full time, office based in Berkshire
- Program Manager
My client is a market leading pahramceuitcal company within their specialist field. They have a new position for an experienced Program Manager / Project Manager. This is an office based position, with senior responsibilities reporting in to the Director of Business Development & Strategic Scientific Affairs.
- Project Manager Technical Lead – Genpact Pharmalink, Penzberg, Germany
We are recruiting for an experienced Project Manager with prior experience working within the healthcare/pharma industries. This is a contract for 6+ months working on a client site in Penzberg, Germany.
- Project Manager Technical Lead – Genpact Pharmalink, Basel, Switzerland
We are recruiting for an experienced Project Manager with prior experience working within the healthcare/pharma industries. This is a contract for 6+ months working on a client site in Basel, Switzerland.
- Regulatory Affairs Manager
The primary responsibility of this role is to lead the EU regulatory affairs team, the creation of regulatory documents and development of regulatory strategy to achieve regulatory approvals and clearances worldwide expediently and consistently within all studies, interventional and non-interventional.
- Regulatory Information Management, Manager
Have you got a background in Life Science or similar degree? Do you bring a strong eye for detail coupled with an analytical mind, with experience in the pharmaceutical industry? You might be just what we're looking for.
Teva are looking for a Regulatory Information Management, Manager who will have responsibility for leadership of significant technology and process projects impacting Global Regulatory Affairs and its partner organisations.
- **Senior Manager PVG & GCP Quality Assurance** - Switzerland
A leading Global pharmaceutical company based in Switzerland are seeking a Senior Manager of PVG and GCP Quality Assurance. The role requires an experienced PV and GCP audit and management professional, who is keen to progress their career into an already successful organisation. This role can provide the opportunity to hands-on audit and also manage and guide professionals in your sector.