iconplc - IT - Administration

Join ICON plc, a global clinical research leader, as a Clinical Research Associate in Reading, UK. You will manage phase I-IV trial sites, ensuring GCP compliance and successful study delivery. This role requires monitoring experience and offers competitive benefits with significant travel.

Join ICON plc as a Senior Clinical Research Associate in Reading, UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insuran...

Join ICON plc as a Freelance Senior CRA in Prague. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. Requires fluency in English & Czech, extensive CRA experience, and 60% travel. Enjoy competitive benefits including health insurance and a global support program.

Join ICON plc as a Clinical Research Lead Assistant and help shape the future of clinical development. This remote role requires strong organizational skills, fluency in English, and proficiency in Microsoft applications to provide key administrative support for clinical trials. We offer competit...

Lead global clinical trials from start-up to database lock as a Senior Clinical Trial Manager at ICON in Boston. Utilize your 10+ years of experience to oversee budgets, drive enrollment, and mentor CRAs. This pivotal role offers competitive health insurance, retirement planning, and a chance to ...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health in...

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee global oncology trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Associate in Singapore. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires 2+ years of CRA monitoring experience, a relevant degree, and 60% travel readiness. We offer competitive health insurance, retire...

Join ICON plc as a Clinical Research Associate II in Ankara. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement plans,...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II/Senior CRA in Belém do Pará. You will design trials, analyze complex medical data, and advance innovative therapies. We seek a degree holder with solid CRA experience in CRO/pharma and deep ICH-GCP knowledge. En...

Join ICON plc, a global clinical research leader, as a Contract Analyst I in Warsaw. Utilize your 5+ years of CRO/pharma contract negotiation experience to prepare and finalize clinical trial agreements and budgets. This role offers competitive benefits, including health insurance and retirement ...

Join ICON plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and site management expertise in a world-leading CRO. Enjoy competitive benefits...