Clinical Research Associate

🔥 12 hours ago

🍂 Massachusetts, Pennsylvania, +1 more states – Remote

🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote 🤠 Texas – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 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.

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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

• Monitor progress of clinical studies at the site level to verify subject rights and well-being, data accuracy and completeness, and compliance with protocol, SOPs, ISO/GCP, and applicable regulations • Provide on-site and remote support during clinical trial start-up, enrollment, follow-up, and closure • Review subject source documents and ensure protocol requirements are met and reported • Compare Case Report Form data against source documents and verify informed consent forms • Review regulatory documents and device accountability records; investigate and resolve data discrepancies • Communicate with clinical sites and project team members through monitoring reports, follow-up letters, study memos, and correspondence • Train site personnel and maintain site personnel, qualification, and training records • Address, document, and escalate site non-compliance issues; support regulatory inspection activities • Identify, document, and report reportable events • Participate in study-specific meetings, teleconferences, and trainings • Collaborate with cross-functional team members and study sites throughout all study phases • Work with the In-house CRA team to collect and review investigator/site documentation and approve applicable database documents

🎯 Requirements

• Minimum of 1 year of medical device experience • Minimum of 2 years of site monitoring experience • Bachelor's degree or Registered Nurse (RN) qualification • Ability to travel up to 60% • Therapeutic experience aligned with at least one Boston Scientific division: Interventional Cardiology, Cardiac Rhythm Management, Cardiac Electrophysiology, Neuromodulation, Urology, or Endoscopy • Proficient with MS Office skills (Word, Excel, PowerPoint, Teams) • Prior experience with Medidata RAVE and VEEVA Vault preferred • The candidate should be based in or near Philadelphia, Boston, or Dallas • 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