Clinical Research Associate I

🔥 15 hours ago

🌐 Poland, Spain, +1 more countries – Remote

🇵🇱 Poland – Remote 🇪🇸 Spain – Remote 🇷🇸 Serbia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 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

• Ensure quality of data submitted from study sites and assure timely submission of data • Provide appropriate reporting and follow-up for all safety events by site personnel • Ensure completeness and compile regulatory and ethical submission documentation, including IRB approval, informed consent, and lab certification • Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF) • Perform feasibility studies and site identification activities for potential sites as requested • Collaborate remotely with clinical operations teams, colleagues, and sponsor contacts

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills • Ability to contribute to a team remotely • Strong customer focus and ability to interact professionally with a sponsor contact • Proficiency in Microsoft Office, CTMS, and EDC Systems • Two-year college curriculum or equivalent education/training and one year of experience with clinical research or other relevant experience • Proficiency in English and Polish and one other language: German, French, Italian, or Spanish

🏖️ 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 • Supportive, team-oriented work environment • Hands-on, accessible leadership • Diverse and inclusive workplace • Remote work arrangement