Senior Clinical Trials Associate

🔥 5 hours ago

🇹🇼 Taiwan – 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

• Coordinate and track project team system access • Maintain project portals and perform documentation quality checks • Support preparation, management, and shipment of clinical trial documentation, including Investigator Site Files • Manage version control and quality review of project documents • Ensure timely submission of documents to the Trial Master File • Track key project information, including site communications and medical question logs • Prepare and distribute meeting minutes for sponsor, project, and internal management meetings • Maintain site and study personnel records • Coordinate project-specific training activities and monitor completion • Contribute to onboarding, coaching, training, and leadership of Clinical Trial Associates • Support continuous process improvement initiatives • Collaborate with Project Managers, CRAs, and cross-functional study teams across multiple clinical projects

🎯 Requirements

• Degree-level qualification or equivalent experience • Minimum of two years of experience in a related role • Proficiency in English and fluency in the local language of the country of location • Strong interpersonal skills • Ability to collaborate effectively across project teams • Ability to work independently with minimal supervision while contributing as a team member • Strong organizational, problem-solving, and multitasking skills • Excellent attention to detail and commitment to quality • Ability to mentor, coach, and support colleague development • Working knowledge of ICH, GCP, and applicable FDA or EU regulatory requirements • Strong proficiency in Microsoft Outlook, Word, Excel, and PowerPoint

🏖️ 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 and cohesive teams • Accessible leadership • Opportunities for onboarding, coaching, training, and leadership development