Responsible for the development and execution of key aspects of the European marketing strategy and tactics for one of the Ophthalmology category, Gla...
As Clinical Programmer you will be involved in supporting global data handling activities by providing study databases and reporting tools for clinica...
The UK Clinical Projects Group, within the Medical Affairs Department is a rapidly evolving team of Project Managers and Clinical Trials Assistants de...
We are recruiting for the position of Senior Quality Rick Specialist to join our international team.
Reporting to the Principle Team Lead for Service...
You will apply your extensive experience in pre-launch marketing to maximise the potential value of a variety of pipeline products. You would be the ...
To further strengthen our national Regulatory Affairs group, part of the Medical Department, we have an exciting opportunity for an experienced regula...
You’ll draw on your experience of multiple sclerosis as you work to develop market insight to shape positioning and develop pre-launch brand strategie...
A new opportunity has arisen to join the Clinical Data Management team. We are recruiting for a Study Data Manager to take the lead for the planning a...
As a member of the Marketing Insight and Analysis Group (MIAG) you will make an important contribution to the successful marketing and selling of the ...
Here is an exciting opportunity within our Quality Department. We are recruiting for Principal Systems Validation Analyst to provide expertise in supp...
You will be responsible for the production of non-CRF data collection, specification, documentation and for defining the study specific non-CRF data h...
Provide medical/safety expertise to project teams, including communicating information regarding drug safety regulations and any changes that have occ...
University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution...
You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission ha...
Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in colla...
We are currently seeking a proactive, driven Project Manager with experience in Drug Safety to join our expanding Safety team in our Maidenhead office...
Using an evidence-based approach, work with relevant business development staff and
operational leaders to design innovative, but practical and fiscal...
The primary activity of the SAS Programmer is to develop and review SAS® programs and output for the management and reporting of clinical trial data. ...