Senior Clinical Research Associate

🕒 September 3

🇨🇦 Canada – 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 research activities at sites participating in Worldwide Clinical Trials’ clinical research projects • Participate in all stages of clinical studies, including site identification, study start-up, regulatory document collection, contract and budget negotiation support, site training, study maintenance, and site closeout • Conduct study initiation visits (SIVs) • Perform most site management remotely • Ensure compliance with informed consent procedures, safety-event reporting, and applicable regulatory requirements

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC Systems • 5+ years of experience as a Clinical Research Associate OR 4-year university degree OR Nursing Degree • Experience in Oncology/CNS/Rare Disease is required • Candidates must reside in Canada • Willingness to travel regionally required • Bi-Lingual in French and English

🏖️ Benefits

• Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Regular touchpoints and coaching conversations with Line Manager • Clear career path and professional development leading to Clinical Trial Manager roles • Accessible Executive Leadership team • Equal employment opportunities and inclusive workplace