A forensic scientist with DNA specialisation and court experience as an expert witness. Responsible for high throughput reporting of NDNAD matches and...
Develop and implement the product safety strategy and overall risk/benefit assessment,
Integrate, analyse and clinically interpret safety information...
The role will require you to be medically qualified having obtained a medical degree or PhD along with a minimum of 7 years progressive experience in ...
As the Global Auditor Manager you will be joining their global operational excellence team and you will focus on Quality engineering, Global audit man...
Manage assigned geographic territory with regard to sales activities, including: Generate product interest and lead generation by performing cold call...
The FSE will act as an essential interface between the field organization and internal support structure by providing timely onsite technical assistan...
You will have strong organisation and communication skills and a thorough understanding of medical terminology, physiology, pharmacology and the drug ...
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 ...
You will have at least two years experience in a CRO, pharma/biotech outsourcing or software company in a similar role. A Bachelors degree in a busine...
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. ...
The GPM will be responsible for managing International studies in Phases I-IV. This is a client focused role which is pivotal in the success of our pr...
The successful candidate will be expected to know Allergan systems and SOPs to a good level, and really focus on CRA performance / generate metrics /...