ICON plc is a global leader in drug and device development, providing innovative consulting and commercialization services to enhance client outcomes and accelerate market entry.
Dublin
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Remote · United States
Manage the day-to-day operations of assigned Phase I oncology clinical trials to ensure compliance with GCP/ICH guidelines and project goals. Lead cross-functional teams, oversee vendor interactions, manage trial budgets, and ensure the quality and completeness of trial documentation.
Remote · Burlington, Prince Edward Island, Canada
You will oversee and coordinate the end-to-end preparation, negotiation, and execution of clinical trial agreements and budgets. Additionally, you will provide guidance to site contracts negotiators and ensure all deliverables meet quality and timeline expectations.
Remote · Canada
The Study Start Up CRA is responsible for managing site selection, study start-up activities, and ensuring all deliverables meet timelines and regulatory standards. They act as the primary contact for trial sites, facilitating document collection, IRB/IEC submissions, and ensuring inspection readiness.
Hybrid · Toronto
The Clinical Associate will assist in the planning, execution, and monitoring of clinical trials while ensuring adherence to regulatory guidelines and protocol requirements. They will coordinate study activities, manage data collection, and collaborate with cross-functional teams to support successful trial execution.
Remote · Burlington, Prince Edward Island, Canada
The Senior Contracts Manager will review, analyze, and negotiate clinical trial contracts and vendor agreements to ensure regulatory compliance. They will also collaborate with cross-functional teams to assess risks and provide guidance on contract interpretation and dispute resolution.
Remote · Canada, United States
The Clinical Project Manager oversees a portfolio of projects, acting as the primary client liaison to ensure deliverables are met on time and within budget. They lead cross-functional teams, manage project financials, and provide performance feedback to team members.
Remote · Blue Bell, Pennsylvania, United States
The Study Start Up Associate II leads clinical trial initiation activities, including site document collection, review, and activation. They also collaborate with internal teams and CROs to ensure process compliance, track metrics, and resolve site-related issues.
Remote · Blue Bell, Pennsylvania, United States
You will lead clinical trial initiation activities, including site document collection, review, and activation. Additionally, you will collaborate with internal teams and CROs to ensure process compliance and resolve site-related delays.
Remote · Blue Bell, Pennsylvania, United States
You will manage clinical trial site contracting, including budgets, payment terms, and amendments while collaborating with internal teams. Additionally, you will perform invoicing, reporting, and ensure all contract management activities align with project timelines and fair market value guidance.
Remote · United States
The Contract Analyst I will prepare and verify invoicing while managing a portfolio of clinical trial contracts and budgets. They will negotiate site-related contracting items and collaborate with internal teams to ensure study startup metrics and timelines are met.
Remote · Blue Bell, Pennsylvania, United States
The Site Activation Lead manages day-to-day site start-up and activation activities while providing guidance and mentoring to the FSP Site Start Up team. They are responsible for driving study start-up metrics, ensuring adherence to project plans, and collaborating with Clinical Operations to meet enrollment timelines.
Remote · Canada
Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Collaborate with investigators to maintain high-quality clinical data and prepare study documentation.
Remote · Blue Bell, Pennsylvania, United States
The Senior Medical Writer will lead the development and execution of medical writing strategies for clinical research projects, including the preparation of protocols, CSRs, and regulatory submissions. They will also collaborate with cross-functional teams to interpret clinical data and mentor junior staff to foster a culture of excellence.
Remote · Burlington, Prince Edward Island, Canada, Montreal, Quebec, Canada
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
Remote · Burlington, Prince Edward Island, Canada
The role involves reviewing, analyzing, and negotiating contracts and legal documents related to clinical trials and vendor relationships. It also requires collaborating with cross-functional teams to mitigate risks and maintaining accurate contract records.
Remote · Montreal, Quebec, Canada
Monitor the progress of clinical studies at investigative sites or remotely to ensure trials are conducted according to protocol. Ensure all recording and reporting comply with SOPs, ICH-GCP, and applicable regulatory requirements.
Remote · Montreal, Quebec, Canada
Monitor the progress of clinical studies at investigative sites or remotely to ensure trials are conducted according to protocol. Ensure all recording and reporting align with SOPs, ICH-GCP, and applicable regulatory requirements.
Remote · Blue Bell, Pennsylvania, United States
Lead the development of high-quality regulatory and clinical documents, including study reports and protocols. Oversee medical writing workstreams and mentor junior writers to ensure adherence to industry standards and timelines.
Remote · Canada
The Local Trial Manager is responsible for end-to-end trial delivery at the country level, serving as the primary point of contact for internal partners. Key duties include managing local vendors, overseeing milestones from feasibility to close-out, and ensuring inspection readiness.
Hybrid · Montréal
Manage clinical trial administration, including document tracking, eTMF reconciliation, and regulatory submissions. Handle financial duties such as developing site budgets, negotiating contracts, and executing payments to investigators and vendors.
