Senior Clinical Research Associate – CNS

Job not on LinkedIn

🔥 0 minutes ago

🇨🇿 Czechia – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 25%

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.

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Lifelancer

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2020

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Pre Seed Round on 2022-03

Consulting • Healthcare • Logistics

Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

📋 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 processes, and safety reporting expectations • 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

• Must reside within Czechia • Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • Required experience monitoring clinical trials • Willingness and ability to travel within the specified region, approximately 6–8 days per month • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements

🏖️ 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 • Home-based/remote work arrangement • Global team collaboration • Supportive, cohesive teams and accessible leadership • Diverse and inclusive work environment • Employee opportunity to influence clinical study success and support high-quality study delivery