10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź 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.
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10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź 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.
âą Contributing to clinical trial monitoring activities, taking responsibility for 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
âą Bachelor's degree in a scientific or healthcare-related field âą Minimum of 2 years of experience as a Clinical Research Associate 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%)
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 Nowđ June 11
Clinical Research Associate monitoring and ensuring the progress of clinical studies at investigative sites. Responsible for coordinating study setup and compliance with protocols and regulations.
đ«đ· France â Remote
đ° $75M Private Equity Round on 2015-12
â° Full Time
đą Junior
đĄ Mid-level
đŹ Research Analyst
đ June 11
1001 - 5000
đ§Ź Biotechnology
âïž Healthcare Insurance
đ Pharmaceuticals
CRA overseeing clinical studies with a focus on site visits and regulatory compliance. Join Precision for Medicine, a leader in life sciences, with a strong emphasis on oncology and rare diseases.
đ«đ· France â Remote
đ° $35.2M Venture Round on 2021-03
â° Full Time
đą Junior
đĄ Mid-level
đŹ Research Analyst
đ June 11
Clinical Research Associate at PSI responsible for onsite monitoring and study progress communication. Collaborating with internal teams and supporting regulatory preparations across clinical studies in various therapeutic indications.