iconplc

Lead clinical data science initiatives for a world-leading CRO. Ensure data quality and integrity across studies from setup to database lock. Requires 6+ years' lead experience, including study start-up and 5+ database locks. Competitive benefits and flexible location options in Johannesburg, Rea...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Raleigh or Blue Bell. Utilize your CRO/pharma experience to manage vendors and support study start-up activities. This role offers competitive benefits, including health insurance and retirement planning, in a dyna...

Join ICON plc as a Clinical Scientist I in Sao Paulo. Design and conduct pivotal clinical trials, applying your advanced life sciences degree and research experience. Collaborate with global teams to develop innovative therapies and enjoy comprehensive health and retirement benefits.

Join ICON plc as a Biostatistician II and help shape the future of clinical development. You will support study design, statistical analysis, and reporting under senior guidance. This role requires a Statistics degree, industry experience, and proficiency in statistical software. We offer competi...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Vienna. 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 insura...

Join ICON plc in Sao Paulo as a Senior Investigator Pricing Analyst. You will develop and analyze pricing strategies for clinical trial investigators, utilizing your financial analysis and modeling expertise. This role requires experience in cost management within healthcare or clinical research....

Join ICON plc as a Clinical Research Associate in São Paulo. Oversee clinical trial activities, ensuring protocol and GCP compliance across multiple sites. This sponsor-dedicated role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health ins...

Lead clinical trials from planning to completion as a Clinical Trial Manager at ICON Plc. Oversee timelines, budgets, and regulatory compliance while collaborating with cross-functional teams. This role requires a science/medicine degree, therapeutic expertise, and offers competitive benefits inc...

Lead patient recruitment strategies for clinical trials at ICON plc in Reading. Utilize your 7+ years of experience in clinical research and digital marketing to enhance patient access and engagement. You will analyze metrics, lead cross-functional teams, and build key partnerships. We offer comp...

Join ICON plc as a Senior CTA and shape the future of clinical development. You will assist in designing and analyzing trials, interpret complex data, and advance innovative therapies. The role requires a scientific degree, clinical research experience, and excellent organizational skills. We off...

Join ICON plc as a Clinical Supplies Manager in Warsaw. You will oversee clinical trial supply projects, ensuring regulatory compliance and timely delivery. This home-based role in Poland requires a relevant degree and proven pharmaceutical supply chain experience. We offer competitive health ins...

Join ICON Plc in Paris as a Clinical Research Associate I. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel. We offer health insurance, competitive retirement plans, and a global...