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...
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...
As Clinical Programmer you will be involved in supporting global data handling activities by providing study databases and reporting tools for clinica...
The successful candidate will have four to six years’ experience in a CRO, pharmaceutical or finance/operations environment and at least a year as a d...
Responsibilities include improvement and development of operational and financial processes, management of our central information system and regular ...
In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
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. ...
In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
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. ...
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. ...