ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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.
Clinical Research Associate
đ„ 4 hours ago
đ Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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.
đ Description
âą You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. âą Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. âą Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. âą Collaborating with investigators and site staff to facilitate smooth study conduct. âą Performing data review and resolution of queries to maintain high-quality clinical data. âą Contributing to the preparation and review of study documentation, including protocols and clinical study reports
đŻ Requirements
âą Bachelor's degree in a scientific or healthcare-related field âą Minimum of 2 years of experience as a Clinical Research Associate after being certified âą In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines âą Strong organizational and communication skills, with attention to detail âą Ability to work independently and collaboratively in a fast-paced environment âą Willingness to travel as required (approximately 60%)
đïž Benefits
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
Apply Now
