iconplc

Join ICON, a world-leading clinical research organization, as a Contract Senior Clinical Research Associate in Los Angeles. This 6-month role requires 3+ years of independent monitoring, ICH-GCP expertise, and 80% travel. You will oversee site visits, ensure protocol compliance, and drive data in...

Join ICON as a Clinical Sample Processor I in Whitesboro, US. You’ll manage daily sample shipments, perform data entry, barcode labeling, and quality checks in a lab setting. Requires a High School Diploma, computer skills, and attention to detail. Enjoy competitive benefits including health insu...

Join ICON as a Sr. TMF Specialist in Raleigh, NC, and ensure clinical trial document accuracy. Leverage 2+ years of TMF experience and a life sciences degree to manage document integrity, conduct audits, and support cross-functional teams. Enjoy benefits like health insurance, retirement planning...

Seeking a Clinical Study Lead in Boston, Basking Ridge, or Philadelphia. Leverage 5+ years of experience, including 3 years in management, to oversee CROs and vendors. Ensure protocol adherence, budget timelines, and strong site relationships. Enjoy competitive benefits, health insurance, and ret...

ICON plc seeks a Talent Sourcing Recruiter in Raleigh, NC, to build robust pipelines for critical roles in clinical research. You will proactively identify and engage candidates using sourcing tools, social media, and networking. Ideal candidates have recruiting experience in life sciences or hea...

Senior CTA opportunity at ICON in the United States. Ensure clinical trial site compliance with GCP and regulatory standards. Requires a Bachelor’s in life sciences or clinical research, plus strong site management and analytical skills. Benefits include health insurance, retirement plans, life a...

Join ICON Plc as a Clinical Research Associate and oversee clinical trials across multiple US locations. Leverage your expertise in GCP, site management, and regulatory compliance to ensure data integrity and quality. This role requires a Bachelor’s in a scientific field, 60% travel, and strong p...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Lead Clinical Research Associate (CRA) specializing in Ophthalmology at ICON plc. Lead site management, mentor CRAs, and ensure ICH-GCP compliance across complex trials in the United States. Requires a life sciences degree and extensive CRO experience. Enjoy competitive benefits including health ...

ICON seeks a Clinical Research Associate II in Nanjing, China, to design and analyze clinical trials, ensuring protocol compliance and patient safety. Requires a Bachelor’s in science/healthcare, 2+ years CRA experience, and ICH-GCP knowledge. You will conduct site visits, manage data integrity, ...

ICON seeks a Clinical Research Associate II in Shenyang, China, to design and analyze clinical trials, ensuring protocol compliance and patient safety. Requires a Bachelor’s in science/healthcare and 2+ years of CRA experience with ICH-GCP knowledge. You will conduct site visits, manage data inte...

ICON seeks a Clinical Research Associate II in Wuhan, China, to design and analyze clinical trials. You will conduct site monitoring, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree and 2+ years of CRA experience. Enjoy competitive benefits, health insurance,...