Clinical Research Associate

November 23

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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 trial sites. • Monitor clinical trials according to ICH guidelines and GCP. • Collaborate with Clinical Operations Manager to ensure timelines and quality standards are met. • Support feasibility, site identification, training, monitoring visits, and reporting.

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 & Polish (writing and speaking).