ICON plc
Jobs at ICON plc
Let Your Resume Do The Work
Upload your resume to be matched with jobs you're a great fit for.
Success! We'll use this to further personalize your experience.
Recently posted jobs
Healthtech • Biotech • Pharmaceutical • Manufacturing
Manages sales operations by analyzing performance, pipeline, forecasting, and market data; developing dashboards, reports, and forecasting models; improving sales processes and data governance; supporting commercial tools and systems; partnering with Sales, Finance, Business Development, and Operations leaders; leading continuous improvement; and coaching junior team members.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Project Manager, IRT oversees IRT system activities, ensuring timelines and budgets are met, while managing stakeholder communications and risks.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Supports clinical development programs by negotiating and executing contracts with ancillary vendors. Manages confidentiality agreements, scopes of work, study assumptions, budgets, payment structures, invoicing, reconciliations, risks, and stakeholder relationships. Requires clinical trial budget development experience, pharmaceutical industry knowledge, and familiarity with GCP, GDPR, and data privacy. The role also maintains contractual and operational processes and manages vendor engagements through post-contract oversight.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Coordinates clinical site contract execution, including routing agreements for signature, quality control, distribution, electronic filing, Medidata entry, reporting, and CDA negotiations. Serves as a liaison among investigative sites, vendors, legal teams, and internal stakeholders. Supports inspections and audits while maintaining accuracy, compliance, and effective communication in a cross-functional matrix environment.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead global clinical trials end-to-end: design and implement protocols, manage day-to-day operations, ensure regulatory compliance, analyze and interpret trial data, resolve operational challenges, and coordinate internal and external stakeholders to optimize study enrollment and outcomes.