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Background: job role: this role may act as lead clinical data manger or will provide support to the lead cdm for one or more projects. responsibilities will include mentoring junior staff and providing work direction on all associated tasks within a project as well as being responsible for the administrative and financial oversight of designated projects. principal activities / duties include: •...
Job date 01-12-2008 20:00:00  Source: Inpharm 

Background: blue pelican pharmaceutical's client; a global pharmaceutical business is seeking a contractor to provide medical information services for an initial twelve month contract period. primary duties: the duties will centre on; copy approval phone and face to face contact with health care professionals some medical writing qualifications: a life science education (ideally with a post gradua...
Job date 01-12-2008 13:00:00  Source: Inpharm 

Background: i have a client who is looking for experienced cra's to work homebased in the uk and ireland. this is for a brand new cardiovascular mega trial to start in january 2009. the ideal candidate will have the following; minimum 2 years monitoring experience. cardiovascular experience is prefered but not essential. be available to travel nationwide, for monitoring visits. be set up to work f...
Job date 01-12-2008 10:00:00  Source: Inpharm 

Background: my client is a global pharmaceutical company they are looking for a clinical project manager to work on an initial 6 month contract. you will be responsible for all project management activities related to clinical trials in accordance with ich gcp and company sops. you will have an input into protocol development in conjunction with the medical manager. planning, forecasting and manag...
Job date 27-11-2008 19:00:00  Source: Inpharm 

Background: looking for a contract role in the south east commutable from london? had experience in clintrial programming and sas? want to be part of a global cro in a highly valued role? the candidate will have had 2years experience within data management and 1 year in clintrial programming within a cro. experience will encompass clintrial 4.2 or 4.4 and sas programming will also be necessary to ...
Job date 25-11-2008 17:00:00  Source: Inpharm 

Background: our pharmaceutical client is looking for a clinical research associate to come and join their expanding team to bring motivation and support to the department. primary duties: as a field-based crs, for given studies, you will be responsible for all aspects of site management from feasibility and site selection to site close. you will work to agreed targets for patient recruitment, data...
Job date 25-11-2008 12:00:00  Source: Inpharm 

Background: our client, a major pharmaceutical company along the m3 corridor has a new opportunity to join this expanding clinical research department. this is a great opportunity to take on a varied role with project management. primary duties: responsibilities include: * develop and implement the agreed clinical study. * co-ordinate the study planning, development of key project timelines * m...
Job date 25-11-2008 11:00:00  Source: Inpharm 

Background: looking for a contract role in the south east commutable from london? had experience in clintrial programming and sas? want to be part of a global cro in a highly valued role? the candidate will have had 2years experience within data management and 1 year in clintrial programming within a cro. experience will encompass clintrial 4.2 or 4.4 and sas programming will also be necessary to ...
Job date 24-11-2008 20:00:00  Source: Inpharm 

Background: my client is a global pharmaceutical company they are looking for a field based cra to work on an initial 6 month contract. main responsibilities will include site initiation, feasibility, on site monitoring and close out visits. this is an urgent requirement with an immediate start. please send your cvs in word format. additional information: hobson prior is a specialist employment bu...
Job date 24-11-2008 20:00:00  Source: Inpharm 

Background: this is a management role and pros will lead a registration team in order to obtain and maintain marketing authorisations for new products in designated territories, and other registration activities or be responsible for providing specialist knowledge to support obtaining, and maintaining marketing authorisations for new and existing products, in designated territories, and other regi...
Job date 23-11-2008 21:00:00  Source: Inpharm 

Background: an excellent opportunity for senior regulatory or become a senior regulatory affairs executive at a fast growing cro company where you can learn and work on the full life cycle. enabling you to gain high level regulatory strategy experience. to apply if you would like to discuss this vacancy further, please call steve or sean on +44 (0)1992 764853 / +44 (0) 1992 710805, or email cv@ddr...
Job date 23-11-2008 21:00:00  Source: Inpharm 


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