Company: inVentiv Health Clinical
Location: South East England
Closing Date: 27 Oct 16
Salary (£): Negotiable
Clinical Research Associate II – UK Wide Pharmaceutical companyFull time - Field basedinVentiv Health -Transforming Promising Ideas into Commercial Reality Working fully outsourced to our global pharmaceutical client, the Clinical Research Associate is fully responsible for the successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and int ...
Clinical Research Associate II – UK Wide
Full time - Field based
inVentiv Health -Transforming Promising Ideas into Commercial Reality
Working fully outsourced to our global pharmaceutical client, the Clinical Research Associate is fully responsible for the successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures.
With full ownership of investigator sites for assigned studies across TA's, the Clinical Research Associate will be involved from site feasibility, with responsibility for the management of the site right through to close-out.
- CRAs will typically be responsible for managing 10 -20 investigational sites at any given time, depending upon the nature and complexity of the study.
- Build and maintain excellent working relationships with external personnel directly involved in study conduct and maintains these despite the difficulties that often arise during the course of a clinical study.
- The CRA will maintain a high level of expertise and knowledge in order to project as legitimate role model to be able to participate in the training and supervision of CRAs in study-specific activities, to ensure uniform study conduct and centre management.
The successful candidate will be able to demonstrate prior experience of investigator site management, including conducting monitoring visits, for either a pharmaceutical company or a CRO. Fluency in English is a must, as well as an ability to communicate effectively with others.
This is a home-based role and site location is yet to be confirmed.
This role will be working through inVentiv Health on a permanent basis.
If you have the required experience for this position and are eligible to work in the UK then please apply by CV or contact Amanda Bond on 01628 587 413.
To find out more about our company and search and apply for other open jobs please visit our website http://www.inVentivHealthclinical.com
inVentiv Health is a global professional services organization designed to help the biopharmaceutical industry deliver new drugs and therapies to market. Our combined Clinical Research Organization (CRO) and Contract Commercial Organization (CCO) is made up of more than 14,000 employees who have the ability to service clients in more than 90 countries. We offer a differentiated set of solutions designed to improve client performance and accelerate the process of bringing products to market. For more information, visit inVentivHealth.com
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