- Clinical Project Manager required for Top Global Pharma, Home-based, UK
Our client is a very successful global pharma, Top pharma company to work for and have cutting edge compounds in the market, they are passionate working in Clinical Research and making a difference on a global scale, they too would like you to have this same passion joining them.
This is a full-time opportunity so if you are a Clinical Research Professional who has a mixed background in both Lead CRA/Project Management experience within UK then please read on…
- Junior Clinical Project Manager/Senior CRA – Leading Belgian Biotech firm
An exciting opportunity has arisen for an experienced and highly motivated SCRA to join my client, a leading international biotech firm as the new Senior CRA/Junior CPM. This role will work in close collaboration with the VP of Medical Affairs and Clinical Operations and will assist the current team with the company’s international projects.
- PW 6541 Manager Global Regulatory Affairs Oncology
This global Pharma company are looking for an accomplished regulatory professional to take responsibility for the quality and compliance of regulatory submissions for their attractive oncology portfolio including Clinical Trial Applications, scientific advice briefing packages, paediatric investigational plans and Marketing Authorisation Applications
- PW 6425 Clinical Study Manager, Oncology
Excellent opportunity available for an experienced Study Manager/ Clinical Study Manager to join one of our smaller, global pharmaceutical clients. The ideal candidate for this position will hold an extensive Oncology background and would have worked on international studies looking to gain Clinical Project Management experience within pharma. EU candidates open to a move to the UK are also encouraged to apply.
- PW 6544 Senior Manager, Clinical Operations
This is a high profile, key global clinical ops lead role within the General Medicine Group of this global pharma company. Focus will be on a clinical study for a high priority phase II trial in Neuroscience leading a cross-functional study team to ensure study milestones and deliverables are achieved with quality of data being suitable for regulatory submission.
- Senior CRA - Germany - Phase III Oncology Study - Single-sponsor (Top 5 Pharma)
A home-based Senior CRA position in Germany, working directly for the Sponsor as part of a Global Phase III Oncology Trial.
- Clinical Research Associate (CRA) - Germany - Phase III Oncology Study - Single-sponsor (Top 5 Pharma)
A home-based CRA position in Germany, working directly for the Sponsor as part of a Global Phase III Oncology Trial.
- Clinical Project Manager (Junior/Senior)
Clinical Project Manager (Junior/Senior)Global top 10 CRO providing clinical development services (Phase I to IV) for the pharma industry worldwide.LOCATIONSpain, or ItalyROLE* Manage multi-functional project teams to ensure proper use of study tools/materials and compliance with standard processes.* Create management plans, team assignments, oversight of database maintenance.* Manage communication and reporting schedules with Sponsor.* Gather information on team performance. ...
- Senior Regulatory Affairs Manager Medical Devices EMEA (daily rate contract)
Our client is looking for Senior Regulatory Affairs Manager for Medical Devices EMEA for a 12 month contract position to start ASAP. Experience with Class III medical devices and change control essential. Competitive daily rate of pay.
- PW 6471 Senior Manager, Clinical Outsourcing
This interim role at our client, a global pharma company will have responsibility for leading and managing activities related to the outsourcing of clinical services, negotiation and maintenance of contracts for CROs and technical suppliers. Additionally, the role will manage the processes which support the implementation and management of global outsourcing.