PPDis a leading global contract research organization providing comprehensive,integrated drug development, laboratory and lifecycle management services.
Our customersinclude pharmaceutical, biotechnology, medical device, academic and government organizations.With offices in 46 countries and approximately 23,000 professionals worldwide,PPD applies innovative technologies, therapeutic expertise and a firmcommitment to quality to help customers bend the cost and time curve of drugdevelopment and optimize value in delivering life-changing therapies to improvehealth.
We are activelyrecruiting for a (Senior) Clinical Research Associate to join our growing teamin South Africa, in the Johannesburg office and to be dedicated to only one sponsor .
Job Profile :
The Clinical Research Associate (CRA) performs and coordinates all aspects ofthe clinical monitoring and site management process in accordance with ICH GCP,FDA guidelines, local regulations and Sponsor’s SOPs.
The CRA conductssite visits to assess protocol and regulatory compliance and manages required documentationand ensures that data will pass international quality assurance audits.
Theyalso develop collaborative relationships with investigational sites.
Education and Experience :
PPD Offers :
As an equal opportunity employer, PPD believes that employees are the key toits success, and is committed to your professional growth.
We offer anattractive salary, comprehensive benefits package as well as bespoke personaldevelopment and training programs.
We are a global leader inthe contract research organization (CRO) industry. Certainly an exciting butalso demanding and competitive industry.
We know that to attract the best andthe brightest talent, we have to provide a stimulating and challenging workenvironment.
We also realize we have to take care of our employees since theyare the key to our success.
For more information, please, feel free to visit our corporate web site at : www.ppdi.com
Please note that we are not able to consider applications without any previousexperience in clinical trial monitoring and only suitable candidates will becontacted.