iconplc - IT - Administration

Join a leading life sciences organization as a **Business System Adoption Specialist** in Blue Bell, PA. Leverage your 4+ years of experience in business analysis and change management to drive adoption of clinical trial systems like EDC. We seek a solution-oriented professional with strong prese...

Join ICON plc as an **Evidence Delivery Specialist** in Burlington, Canada. You will ensure inspection-readiness by managing TMF/Master File QC, customizing Expected Document Lists, and collaborating with CROs. Ideal for candidates with a Bachelor’s in life sciences, GCP/ICH knowledge, and strong...

ICON plc seeks a Study Manager in Warsaw, Poland, to drive clinical study delivery within a fully sponsor-dedicated program. Leveraging 3+ years of pharmaceutical experience and ICH-GCP expertise, you will manage end-to-end operations, budgets, and cross-functional teams. This role offers a chanc...

Senior Site Contracts Negotiator sought to lead complex clinical trial agreement and budget negotiations across multiple countries. Join ICON’s dynamic team in Sofia, Warsaw, or Bucharest. Requires a Bachelor’s degree and significant CRO/pharma contracting experience. Enjoy competitive benefits i...

Senior Clinical Research Associate (CRA) needed in Dallas or Houston, TX. Leverage your ophthalmology expertise to oversee multi-site trials, ensuring GCP and regulatory compliance. This role demands strong site management, data integrity, and travel (60%). Join ICON Plc for competitive benefits,...

Senior CRA opportunity in Philadelphia with ICON Plc. Manage clinical trial sites, ensure GCP and regulatory compliance, and drive data integrity. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Enjoy competitive benefits including health ...

Senior CRA opportunity in Seoul, South Korea with ICON Plc. Manage clinical trial activities, ensure GCP compliance, and oversee multiple sites. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health insurance, ret...

Join ICON as a Site Contract Negotiator in Seoul, South Korea. Support the review and negotiation of clinical trial agreements and budgets, ensuring accurate contract execution for timely study start-up. Ideal for candidates with a Bachelor’s degree and initial experience in contracts or clinical...

Senior Clinical Research Associate opportunity in Raleigh, NC with ICON Plc. Manage and monitor clinical trial sites, ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health i...

ICON plc seeks a Supplier Performance Monitor in Raleigh, NC, to oversee data quality and compliance for clinical trials. Ideal candidates possess laboratory auditing experience, with in-vitro diagnostics preferred, and relevant degrees plus 3-12 years of experience. This role involves monitoring...

Join ICON as a Site Management Associate I in São Paulo, Brazil. Support clinical trial site monitoring, ensure GCP compliance, and assist with documentation and data tracking. Ideal for candidates with a life sciences degree and strong organizational skills. Enjoy benefits like annual leave, hea...

Join ICON as a Site Management Associate (IHCRA) in Bogota, Colombia. Support clinical trial site monitoring, ensuring GCP and regulatory compliance. Ideal for candidates with a Bachelor's in life sciences and clinical research experience. Enjoy competitive benefits including health insurance, re...