Clinical Scientist – ONC, ID, Vac, Neuro, Cardio, IMM

Job not on LinkedIn

🕒 March 11

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 55%

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.

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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

• Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management • Support a single study or multiple studies • Lead a study with limited scope, such as Survival Follow-up • Interact with internal and external stakeholders, including study sites and committees, in support of clinical study objectives

🎯 Requirements

• BS/BA/MS/PhD in Life Sciences with 2+ yrs relevant career experience • If no degree in Life Sciences, must have significant experience in clinical development (>5 years) • Experience in Oncology, ID/Vac, Neuro, Cardio, and/or Immunology required • 2 years medical monitoring experience highly preferred • ePro experience a plus • Demonstrated oral and written communication skills • Excel and PP experience required • Ability to travel up to 15% (might include international travel) • Legally authorized to work in the United States and/or Canada • Must not require, now or in the future, sponsorship for employment visa status

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways