An Associate Clinical Study Manager is required for a leading global pharmaceutical company to coordinate international clinical operations and the activities of project teams in a supporting capacity to a Clinical Project Manager. This is ideal for junior level Project Managers or lead/principal CRAs looking to advance project management. The position is initially a 12 month contract, office-based and full-time, as well as offering the opportunity to become a permanent staff.
Regulatory Affairs Lead \ Regulatory Affairs Project Manager - Study Site Start up
Do you want to work for a leading CRO and be home based?
Are you fed up of commuting and sitting in traffic?
Would you like to take the lead and be client facing?
Would you like a Â£55,000 per annum salary plus benefits?
So you have Clinical Regulatory background?
A great opportunity within a world leading pharmaceutical company for a Junior Project Manager or a Lead CRA looking to progress to project management. Key responsibilities will include working in a supporting capacity with a Senior Project Manager to coordinate international clinical operations and the activities of project teams. The position is a rolling 12 month contract, office-based and full-time. For ideal candidates, career progression is a realistic prospects.
A multi-national pharmaceutical company currently carrying out a global recruitment drive following strong financial results is seeking an Associate Director, Project Management to join their study management group within the UK, focused on the delivery of Phase II-III studies and the leadership of the companyâ€™s study management team in the UK. This position is office based out of my clientâ€™s office in Cambridge. ...
A late phase Clinical Project Manager is required for a leading global CRO. Principal duties include independently coordinating and managing the full cycle of multiple studies across different therapies, from initiating project start-up and multi-million budget management to execution, maintenance and conclusion. The role is permanent, home-based, full- time.
A Clinical Project Manager or a Senior Project Manager is required for a leading global CRO. Principal duties include independently coordinating and managing the full cycle of multiple studies across different therapies, from initiating project start-up and multi-million budget management to execution, maintenance and conclusion. The role is permanent, home-based, full- time.
Fantastic new 3-6 month Contract Clinical Operations Leader / PM opening has become available to join this growing, mid-size CRO for their UK team. The position offers home based flexibility, ideally based around the South East or Manchester area and the role is covering investigator led studies in the Oncology field. Managing sites in these locations, principal investigator interaction and PM responsibilities for clinical aspects.
Lead CRA, Clinical Operations Leader, Project Manager â€“ New contract has become available with this growing, mid-tier CRO for a Clinical Operations Leader / Lead CRA. The position is home based in the UK and looking for you to assume site management responsibilities into investigator led studies into the Oncology field.
This requires someone with experience in Investigator led studies and proven oncology exposure at Lead CRA levels or above.
CRAI/CRAII required for an exciting new position with a Global CRO - this role is fully comitted to one sponsor. If you are a Clinical Research Associate with 18 months+ experience and looking for a new challenge you can be rewarded with a generous salary and benefits package, flexible working arrangements and unequalled training and career development opportunities. We are looking for someone who is home based in North of Poland.
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