This is a varied and challenging Clinical Research Associate (CRA) or Senior Clinical Research Associate (SCRA) position with an expert consultancy company!
Broaden your scientific knowledge within clinical research by working on novel studies in phase I-II and Proof of Concept stages of development! When you work for this small but expanding speciality company you take on a broad set of responsibilities ranging from protocol and Investigator Brochure development through to business operations and training!
You ll gain broader exposure in this company than with any other business in the clinical research industry! Based from the office in East Anglia you will work as part of small, highly experienced and dedicated team to deliver clinical projects on time and within budget.
In this small company the CRA and SCRA roles involve site management and monitoring in the UK; study design and set up; the development of regulatory documentation such as investigator brochures, protocols, informed consent and clinical study reports; and business operations activities to include client relationship management, business development and marketing. At the CRA level you will focus mainly on the site management and co-ordination activities and at SCRA level you will be more involved in local project management activities and the development of regulatory documentation in addition to managing sites.
Who are we looking for? With a strong scientific background you will have a proven track record in the management and monitoring of UK sites. Exposure to phase I/II and Proof of Concept is an advantage. Your experience could come from academia, CRO or pharmaceutical/biotechnology company environments.
For more information, please email Kristina on kristina@seltekconsultants.co.uk or call 01279 657716
Job Ref: 8132
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