Senior Clinical Trials Associate

🔥 10 minutes ago

🌐 Argentina, Mexico – Remote

🇦🇷 Argentina – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

✨ Associate

👻 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

• Arrange and track system access for project team members, including Project Managers, Lead CRAs, and CRAs • Maintain and quality audit project portal documents to ensure the most recent revisions are available • Assist with preparation and shipment of clinical trial documentation, including Investigator Site Files • Maintain version and quality control of project documentation and submit documents to the trial master file • Track and maintain project-related information, including site medical question and answer logs • Generate and distribute minutes for project-related meetings, including Sponsor and Internal Management meetings • Provide administrative and project tracking support to clinical project teams • Ensure assigned project tasks are performed timely and accurately

🎯 Requirements

• Excellent written and verbal English • Fluency in the language of the country of location • Strong interpersonal skills • Strong attention to detail and focus on quality of work • Strong organizational and problem-solving skills • Degree level qualification or equivalent experience • Minimum of two years’ experience in a related role • Skill sets and proven performance equivalent to the above

🏖️ 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 • Diverse and inclusive work environment • Supportive teams and accessible leaders • Opportunities to collaborate and be creative