Clinical Research Associate

2 days ago

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Business Wire

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

501 - 1000

Description

• Execute clinical monitoring activities at clinical trial sites • Monitor trials according to ICH guidelines and GCP • Collaborate with Regional Clinical Operations Manager to ensure timelines are met • Conduct feasibility, site identification, selection and monitoring visits • Identify areas for improvement and propose CAPA • Mentor junior staff and CRA(s)

Requirements

• BS in a relevant scientific discipline • Minimum of 2 years of monitoring experience • Experience in oncology global trials preferred • Fluent in German & English (writing and speaking) • Up to 60% travel required

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