10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
đ„ 0 minutes ago
đ§đŹ Bulgaria â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
Where this job comes from
Posted on ICON plc's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
âą Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. âą Ensure protocol compliance, data integrity, and patient safety throughout the trial process. âą Collaborate with investigators and site staff to facilitate smooth study conduct. âą Perform data review and resolution of queries to maintain high-quality clinical data. âą Contribute to the preparation and review of study documentation, including protocols and clinical study reports. âą Take responsibility for clinical trial monitoring deliverables and work collaboratively in a sponsor-dedicated model.
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 Legal right to work in Bulgaria.
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 NowImprove your chances of getting an interview by checking your resume score before you apply.
đ„ 1 hour ago
Clinical Research Associate monitoring investigative sites and supporting clinical trial compliance for AbbVie. Advancing innovative medicines through recruitment, data integrity, safety, and site partnerships.
đ August 27
Clinical Research Associate II advancing AbbVieâs innovative medicines through compliant clinical trials. Managing investigative sites, monitoring study execution, recruitment, data quality, and patient safety.
đ June 25