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Job #02621

About our client Our client is a well-established CRO with global reach, an experienced management team and a loyal customer base. They have developed an industry-wide reputation for a positive work environment and an aggressive training program that ensures employees are up to date on current trends and best practices. This is a strong opportunity for someone that wants to put their drive and initiative to work! Position Location Clinical Research Associate Montreal, Quebec Salary Reports to Highly competitive package, commensurate with experience Management Responsibilities 1) Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance according to company SOPs and client guidelines 2) Generate study specific documentation, including, monitor trip reports, telephone contact reports, site correspondence, and expense reports 3) Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites 4) Review draft protocols for completeness and feasibility 5) Develop CRFs for clinical trials 6) Prepare and process Serious Adverse Event (SAE) reports 7) Resolve queries of CRF data with study site personnel 8) Review tables and listings generated from study data Requirements 1) Bachelor’s degree or RN 2) Minimum 2 years of experience in field monitoring for a pharmaceutical/biotech company or CRO 3) Experience in oncology a plus 4) Ability to manage time and work independently 5) Excellent organizational skills 6) Superb communication (written and verbal) skills 7) Willingness to travel – up to 60%