Senior Clinical Research Associate

November 27

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Public Relations • Press Release Distribution • Investor Relations • SEC filing • SEO

501 - 1000 employees

Founded 1961

Description

• Execute clinical monitoring activities at clinical trial sites. • Monitor clinical trials in accordance with ICH guidelines and GCP. • Identify gaps and areas for improvement and propose CAPA. • Support start-up and provide local expertise. • Collaborate closely with the Regional Clinical Operations Manager to ensure study timelines are met. • Manage sites and site performance by tracking various submissions and resolving data queries. • Conduct monitoring visits and complete visit reports.

Requirements

• BS in a relevant scientific discipline and minimum of 2 years of monitoring experience. • Experience in oncology global trials preferred. • Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines. • 2-5 years of (CRA) monitoring experience in the pharmaceutical or CRO industry. • Experience in oncology/hematology trials preferred. • Excellent communication and interpersonal skills. • Excellent organizational skills and ability to prioritize and multi-task. • Fluent in English & French (writing and speaking).