Senior Clinical Research Associate

🕒 April 29

🏄 California, Florida, +2 more states – Remote

🏄 California – Remote 🐊 Florida – Remote 🔔 Pennsylvania – Remote 🤠 Texas – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

What it means: the chance that no one is really hiring for this job.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

• Support 1study in the cardiovascular/electrophysiology medical device space. • Indication is A-fib. • The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered. • Ability to cover up to 65% regional travel. • Located in the US near a major airport.

🎯 Requirements

• 3 years of monitoring experience required. • A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science. • In-depth knowledge of FDA regulations and ICH/GCP guidelines. • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly. • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams. • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely. • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment. • Ability to work independently and manage multiple priorities in a dynamic environment. • A well-executed plan for communication with the study teams and sites. • Well-versed in clinical trial management. • They are rigorous, detail-oriented, and precise in their reports.

🏖️ Benefits

• Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs. • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

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