Medical Affairs Manager - UK & Ireland
An opportunity for a medical affairs physician looking to progress into a role with scope for European responsibilities and a major therapeutic unit for an established and driven pharmaceutical business. Sitting as part of the European medical team for the Therapy Area who will work in a demanding role with a heavy commercial remit.
Senior Clinical Project Manager/PM/Study Manager: This is a great opportunity for a Clinical Project Manager to join a friendly organisation and gain experience at a small CRO. You will be overseeing clinical project timelines, budgets and milestones on a large phase III trial so previous experience is a must. As a Senior Project Manager you will also be very much involved with building the sponsor relationship.
Study Start Up Associate/Specialist: This CRO is continuing its expansion in Europe following a great 2013 and they are currently looking for a Study Start Up Associate to join their team in South East England. You will be covering MHRA and EC submissions across a range of therapeutic areas. Ideal for a Start Up Associate with strong experience in regulatory submissions looking to gain experience at a slightly smaller CRO with a great team atmosphere and company culture.
*** New Study Manager Opportunity ***
A large international pharmaceutical company with an impressive pipeline in the Cardio-renal therapeutic area is seeking an experienced Clinical Study Manager to join their Study Management team on a 12 month rolling contract basis. This role is fully office based just west of London with flexible working hours around 10am-4pm.
Principal Statistician â€“ Contract up to Â£500 a day
South East, UK or US
Principal Statistician required for 11 month contract role for a global pharmaceutical company. You will be required to provide experienced strategic input, statistical expertise, and leadership to teams in the design of clinical studies and programmes. ...
Senior Clinical Project Manager/Senior CPM/PM: A great mid-sized CRO is looking to further expand their UK CRA team with the addition of an experienced Senior Clinical Project Manager. This is a really exciting role for a PM looking to further their career with the support of a company with an international presence. They offer a stimulating working environment and it is a great opportunity for a Senior PM to join a smaller, close-knit team.
I have an exceptional role for an experienced Clinical Project Manager. I am looking for a home or office based CPM in UK to work on Late Phase clinical trials (peri and post approval). Reporting into the European Head of Project Management.
Opportunity for a dynamic and experienced CPM to join this exciting Niche Pharma Company and take ownership of a global portfolio. Carrying a high level of responsibility, including managing global clinical activity, project planning, acting as senior liaison for external vendors within a cross functional environment and clinical scientific report writing. Offered initially on a 12month fixed term basis, there is opportunity to move to headcount thereafter. <.b>
Senior Study Start Up Associate/Regulatory Specialist: This CRO is continuing its expansion in Europe following a some great business wins and they are currently looking for a Regulatory Affairs Specialist to join their team in the M4 corridor. You will be covering CTAs across a range of therapeutic areas. Ideal for someone with strong experience in regulatory submissions looking to gain experience at a slightly smaller CRO with a great team atmosphere and company culture.
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