Opportunity to join an established and growing Clinical Supplies team within a Blue Chip Pharma Organisation. The role is focused on the EU, however the company is Global and will see interaction and project management at this level. Youâ€™ll provide strategy for protocol development for studies, ensuring delivery. Office based role in London, initially offered on a contract with full likelihood of extension.
Contract, Data Manager, Freelance â€“ 3 x contract Senior Data Analysts (Data Managers) are being sought by this global, top 10 CRO for their Northern England location. The positions will be on 6 month contract basis, view to extensions, focused into data management activities in oracle clinical, paper based studies and EDC.
The contract suits those with proven Clinical Data Manager or Data Coordinator background, keen to work for a global leader and lucrative hourly rate contract.
Opportunity to join a Blue Chip Pharma Organisation as Clinical Supply Program Manager. Youâ€™ll work cross functionally providing clinical supplies strategy for protocol development, establishing appropriate processes within the program. This is a permanent, office based role.
*** Sr. Database Programmer for Clinical Studies â€“ 8 months Contract â€“ Amsterdam - Netherlands *** Contact Marc VdV on +44(0)207-801.33.85
In this role you will be responsible for overseeing and providing advanced technical support related to data management applications required for clinical studies. Furthermore you will be responsible for creating and maintaining study databases for high priority and pivotal studies, Global studies or studies with complex study design.
Our client is a leading biopharmaceutical company with more than 30 operating affiliates worldwide and specialises in respiratory and orphan diseases. With 5 products on the market and a rich pipeline, the company continuously invests in innovation and growth.
i-Pharm Consulting are working on behalf of a leading Pharmaceutical company to recruit for a home-based CRA II/ Senior CRA who can be based at any location in the UK. This company are a global leader within clinical research who have pioneered the discovery and launch of a large number of market leading drugs used throughout the world.
Exceptional opportunity for a leader within global clinical development looking to join the European operations group of a much larger organisation. With the ability to provide agile, specialised expertise in drug development you will play an integral role in leading and managing clinical project personnel and all operational aspects of projects in early clinical development stages.
Established in 1982, Chiltern is a leading global Contract Research Organization with extensive experience in conducting and staffing global Phase I to Phase IV clinical trials across a broad therapeutic range.
Our experienced Team of 1,600 employees located around the world face the daily challenges in clinical trials and offer our clients flexible and efficient solutions as well as high quality in clinical research projects. ...
Clinical Research Associate - Reduced Monitoring- UK
i-Pharm Consulting are working on behalf of a leading Pharmaceutical company to recruit for a home-based CRA to join their operations on a permanent basis. This company are a global leader within clinical research who have pioneered the discovery and launch of a large number of market leading drugs used throughout the world.
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