Description: Our client requires an experience Clinical Research Scientist to assist in the design, implementation, project management and monitoring of Phase I-IV clinical trials. You will be involved in developing study budgets, clinical supplies and materials; managing expenditures and overseeing CROs. You will spend time in the field conducting site termination and other study-related visits and provide clinical support to marketing and sales.

Requirements: We require 2+ years of proven Clinical Research experience in a CRO or pharmaceutical company and working knowledge of Canadian ethical norms and regulations pertaining to clinical studies including GCP, experimental design and sound knowledge of pharmacologic and therapeutic aspects in a variety of therapeutic areas. You must be able to interpret scientific data pursuant to the preparation of study reports and scientific manuscripts. You must have solid interpersonal, written and verbal communication skills and proficiency with relevant software including MS Office and project management tools such as Microsoft Project. Since international travel, including travel to the USA may be required, valid documentation will be necessary. Please note that only applicants satisfying the mandatory Requirements and Education as noted need apply. No telephone calls, please.

Education: University Science Degree - Post Graduate Degree Preferred