10,000+ employees
Founded 1990
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
🔥 0 minutes ago
Where this job comes from
Posted on ICON plc's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago
10,000+ employees
Founded 1990
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
• Serve as a site-aligned end-to-end partner throughout trial lifecycles • Act as the primary point of communication for assigned trial sites, investigators, and site staff • Participate in site feasibility, site qualification visits, follow-up, and final site selection • Lead and coordinate local team activities to meet recruitment targets, data quality, timelines, and study budget • Develop local trial procedures and tools, recruitment plans, contingency plans, risk management, and budget forecasts • Maintain investigator engagement and communicate trial status and issues to stakeholders • Maintain and update trial management systems and analyze trial progress • Initiate corrective and preventive actions when trials deviate from plans • Contribute to site-level recruitment strategy and contingency planning • Manage country-level vendors, invoices, vendor selection, and local study supplies • Conduct local trial team meetings and facilitate study-monitoring training • Prepare and manage country- and site-specific informed consent forms • Ensure adverse events, serious adverse events, and product quality complaints are reported within required timelines • Maintain inspection readiness through complete and accurate trial data and essential documents in CTMS and eTMF/IF • Ensure site data quality and timely query resolution • Support CAPA implementation for audits, inspections, and quality visits • Ensure accurate finance reporting and proactive management of country/local trial budgets • Organize and ensure IEC/HA approvals with the local Start Up team • Provide training or input into process initiatives when applicable • Complete timely and accurate time reporting • Manage and start up complex Early Phase trials with internal matrix clinical teams and sites, as applicable
• BA/BS degree • Degree in a health or science related field • 3 - 5+ years of trial end to end management experience • Start-up & Database Locks/Cleaning experience preferred • HemOnc experience required • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures • Strong IT skills in appropriate software and company systems • Proficient in speaking and writing the country language and English • Good written and oral communication skills as appropriate • Legally authorized to work in the United States • Must not require, now or in the future, sponsorship for employment visa status
• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
🔥 3 hours ago
Senior Clinical Data Manager leading end-to-end data management for Worldwide Clinical Trials’ global clinical research projects. Overseeing data quality, database locks, budgets, risks, and cross-functional delivery.
🇺🇸 United States – Remote
đź’µ $79k - $157k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
🔥 3 hours ago
Program Clinical Data Manager leading complex clinical data management programs for Worldwide Clinical Trials, a global contract research organization. Overseeing data quality, database lock, sponsors, and cross-functional teams.
🇺🇸 United States – Remote
đź’µ $99k - $196k / year
⏰ Full Time
đźź Senior
đź”´ Lead
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
🔥 19 hours ago
Senior Clinical Scientist supporting clinical strategy, trials, data analysis, and publications. Advancing pulsed electric field therapies at biomedical platform Galvanize Therapeutics.
🇺🇸 United States – Remote
đź’µ $145k - $165k / year
đź’° $17.3M Debt Financing - Galvanize on 2019-01
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
đź•’ 3 days ago
Senior Clinical Research Associate monitoring clinical trials for Karius, a genomic diagnostics company detecting pathogens from blood. Managing high-risk sites, compliance, safety, documentation, and corrective actions.
🇺🇸 United States – Remote
đź’µ $91.8k - $137.7k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
đź•’ 3 days ago
Senior Clinical Research Associate advancing Novartis Phase I–IV clinical trials through site monitoring. Managing site relationships, compliance, patient safety, and trial data quality across the western United States.
🇺🇸 United States – Remote
đź’µ $108.5k - $201.5k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor