iconplc - United States, Remote work

Seeking a Senior Local Operations Manager for Oncology Solid Tumor trials in a home-based role in Blue Bell, PA. This position serves as the primary site liaison, driving end-to-end trial management and cross-functional communication. Requires 3-5+ years of trial management experience, solid tumo...

Join ICON as a Site Management Associate I in Raleigh or Blue Bell, US. Support non-client sponsored studies, including Investigator Sponsored Studies, with a focus on operational execution and document tracking. Ideal for candidates with a scientific degree and clinical research experience. Enjo...

Lead global clinical trials as Manager, Clinical Operations at ICON plc in Raleigh, Charlotte, or Blue Bell, US. Leverage 5+ years of CRO/pharma experience and strong GCP knowledge to drive Phase 1-4 study strategies. Manage vendor relationships, budgets, and cross-functional teams with limited s...

ICON plc seeks a Clinical Trial Manager II to lead early-phase oncology trials in the US (Atlanta, Charlotte, Durham, and more). You will manage daily trial operations, vendor setup, and dose escalation safety meetings, requiring 2-3+ years of clinical trial management experience and strong ICH/G...

ICON seeks a Clinical Outcomes Assessment Training Lead in Raleigh, NC. You will design and deliver COA training for clinical studies, requiring a Master’s degree and extensive outcomes research experience. Key skills include advanced PowerPoint, video editing, and strong presentation abilities. ...

Senior Clinical Research Associate – Oncology – East Coast. Lead monitoring of Phase I/II solid tumor trials (gastro, colorectal, breast, head & neck) across the US East Region. Requires 3+ years monitoring experience, 1+ year in oncology, and deep GCP expertise. Enjoy competitive benefits, healt...

Senior Clinical Research Associate sought for Oncology trials in Washington DC. Leverage 5+ years of monitoring experience, including solid tumor and early development trials, to ensure data integrity and subject safety. Manage sites, conduct remote/on-site visits, and mentor junior CRAs using Ve...

Seeking a Clinical Research Associate for multiple US locations. Requires a Bachelor's in science/healthcare and 9+ months onsite monitoring experience with ICH-GCP expertise. You will conduct site visits, ensure protocol compliance, and maintain data integrity. Benefits include health insurance,...

ICON plc seeks a Feasibility Principal Analyst to lead strategic feasibility for rare disease programs across multiple US locations. This role requires 7+ years in clinical research with 5+ years of operational feasibility experience, translating complex enrollment data into actionable recommenda...