Senior Clinical Research Associate

🔥 15 hours ago

⛰️ Colorado, Montana, +2 more states – Remote

⛰️ Colorado – Remote 🦬 Montana – Remote 🌾 Nebraska – Remote 🤠 Texas – Remote

💵 $110.5k - $138.2k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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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

• Work in a sponsor-dedicated model supporting Dermatology & Rare Disease trials • Identify, select, initiate and close-out investigational sites for phase II–IV clinical studies • Ensure adherence to applicable regulations and ICH-GCP principles • Set up and monitor studies independently and proactively • Complete reports and maintain documentation • Submit protocols and consent documents for ethics/IRB approval • Prepare regulatory submissions • Balance sponsor-generated queries • Take responsibility for study cost efficiency • Prepare and review study documentation and feasibility studies for new proposals • Potentially assist in training and mentoring fellow CRAs

🎯 Requirements

• 18 months+ of monitoring experience in phase I-III trials as a CRA • College degree in medicine, science, or equivalent • Previous monitoring experience in medium-sized studies, including study start-up and close-out • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data • Excellent written and verbal communication in German & English • Ability to work to tight deadlines • Availability to travel at least 60% of the time, internationally and domestically • Valid driving license • Legal right to work in the country where the role is based

🏖️ 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 • Career development • Collaborative environment • Annual bonuses reflecting delivery of performance goals