Senior Clinical Research Associate – CNS

🔥 14 hours ago

🇨🇿 Czechia – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies • Identify and assess potential research sites • Coordinate study start-up activities, including regulatory documentation and contract and budget processes • Conduct Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits • Train site personnel on protocol requirements, data collection, and safety reporting • Monitor site performance and provide ongoing support during study maintenance • Ensure informed consent, safety reporting, and regulatory compliance • Partner with sites and study teams to drive data quality, participant safety, and study success • Support site closeout and completion of study requirements

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • Experience monitoring clinical trials • Requires travel within the specified region; 6–8 DOS monthly • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements • Candidates must reside within Czechia • Ability to travel to investigative sites approximately 6–8 days per month

🏖️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law