The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. With truly Global trials in all therapeutic areas, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar!
Key responsibilities of this role include;
* Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
* Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
* Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.
* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
* May provide assistance to more less experienced clinical staff.
At Quintiles we value individuality, fresh ideas, and the contribution that our employees make to our success. In return we offer career opportunities providing flexibility and growth across the organisation, competitive salary and benefits package, work-life balance initiatives and social events. These are just some of the incentives we have to offer.
We are looking for dynamic people who enjoy communicating and interacting within teams, to achieve quality deliverables. Your expertise as a CRA or SCRA will ensure that clinical stages of research projects are completed in accordance with customer high expectations, enabling us to continue our success. Successful candidates will hold a Degree, in a scientific or healthcare discipline complimented by solid prior monitoring experience and lead CRA responsibilities.
