Senior Clinical Research Associate

🔥 1 minute ago

🌐 Canada, United States – Remote

🇨🇦 Canada – Remote 🇺🇸 United States – 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

ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Monitor the progress of clinical studies at investigative sites or remotely • Ensure clinical trials are conducted, recorded, and reported according to the protocol • Ensure compliance with standard operating procedures (SOPs), ICH-GCP, and applicable regulatory requirements • Conduct clinical monitoring activities in study sites or remotely • Support the development of medicines and medical devices through outsourced clinical research services

🎯 Requirements

• Bachelor's degree or international equivalent in a scientific or health-related field, or equivalent combination of education and clinical research experience • Alternatively, authorized healthcare professional qualification such as registered nurse, or equivalent work experience • 1+ years of clinical monitoring experience or equivalent combination of education and experience for the level 2 role • 3+ years of clinical monitoring experience for a level 3 role • Oncology monitoring experience preferred • Ability to travel 70% • Knowledge of ICH and local regulatory authority regulations regarding drug trials • Legally authorized to work in the United States or Canada • Must not require now or in the future sponsorship for employment visa status • Bilingual English/French required

🏖️ Benefits

• Continuous learning culture and professional development opportunities • Competitive base salary • Variable pay and recognition programs • Employee benefits including health and wellbeing programmes, medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Structured training and career pathways • Supportive policies and wellbeing initiatives • Reasonable accommodations during the recruitment process • Equal opportunity and inclusive workplace