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...

Senior Clinical Research Associate (CRA) needed on the West Coast to lead oncology trials at ICON Plc. You will manage multiple sites, ensure GCP compliance, and drive data integrity. Requires a Bachelor's degree, extensive CRA experience, and 60% travel. Enjoy competitive benefits including heal...

ICON seeks a Director, Research Services, Oncology to lead clinical research in Blue Bell, PA. This role drives protocol development, study start-up, and regulatory submissions (FDA/EMA) for solid tumor programs. Requires 8+ years oncology experience, a life sciences degree (Pharm.D./Ph.D. prefer...

Senior Clinical Research Associate sought by ICON Plc to oversee clinical trials across the US. This role requires a Bachelor’s in a scientific field, extensive CRA experience, and expertise in GCP, site management, and data integrity. You will monitor multiple sites, conduct visits, and collabor...