“Full-time Clinical Trial Associate role in Bucharest, Romania (hybrid) at ICON Strategic Solutions. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Salary and benefits package offered. 10% travel required.”
“Full-time Clinical Trial Associate role in Bucharest, Romania, with ICON Strategic Solutions. Requires scientific/healthcare degree and clinical research experience. Hybrid work model. Competitive salary, benefits, and career development in clinical trials.”
“Regular job offer for a Clinical Trial Assistant at ICON Strategic Solutions. Requires a scientific/healthcare degree, clinical research experience, and 10% travel. Offers competitive salary, benefits, and career development in sponsor-dedicated FSP model.”
“Full-time Clinical Trial Assistant role in Madrid, Spain. Requires a Bachelor's degree in life sciences/healthcare, some clinical research experience, and 25% travel. ICON offers competitive salary, benefits, and career development in a sponsor-dedicated clinical trial environment.”
“ICON seeks a Talent Acquisition Business Partner to drive strategic hiring in healthcare/clinical research. Role involves full-cycle recruitment, stakeholder collaboration, and data-driven talent solutions. Competitive salary, benefits, and inclusive culture offered. Healthcare industry experience preferred.”
“Full-time Clinical Data Science Lead role at ICON Strategic Solutions in Mexico. Requires clinical data science experience, statistical modeling, and team leadership. Offers competitive salary, benefits, and career development in clinical trials and data analysis.”
“ICON seeks an eCOA Licensing Associate for Mapi Research Trust to manage client relationships, develop proposals, and ensure eCOA project delivery. Requires expertise in eCOA/COA licensing, technical background, and strong Microsoft Office skills. Competitive salary and benefits included.”
“Remote Clinical Research Associate (CRA II) role at ICON in Barcelona. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Designs/analyzes trials, ensures compliance, and contributes to patient-benefiting treatments. Competitive benefits included.”
“Regular job offer for Study Start Up Associate II in Spain (office or home-based). Requires 2+ years in clinical research, regulatory affairs, and study start-up. Fluency in English and local language plus German/French/Romanian/Dutch. Competitive salary, benefits, and travel (5%).”
“ICON Strategic Solutions seeks a Clinical Research Associate (CRA II) to design and monitor clinical trials, ensuring protocol compliance and patient safety. Requires 2+ years of experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in a global FSP organization.”
“Regular job offer for a Clinical Research Associate (CRA II) role at ICON Strategic Solutions. Requires 2+ years of experience, scientific degree, and 60% travel. Competitive salary, benefits, and career development in clinical trial monitoring.”
“Lead Data Manager role in Mexico at ICON Strategic Solutions. Requires clinical data science experience, statistical modeling, and team leadership. Offers competitive salary, benefits, and career development in clinical trials data analysis.”
“Remote Project Manager role in Mexico for ICON Strategic Solutions. Requires experience in clinical trial management, lab support, and sponsor coordination. Offers competitive salary, benefits, and career development in life sciences/healthcare.”
“Remote position in Mexico for a SMA I role at ICON Strategic Solutions. Supports clinical trial site management, ensures protocol compliance, and requires 25% travel. Bachelor's degree in life sciences preferred. Competitive benefits and career development opportunities included.”
“Graduate Pharmacovigilance Associate role at ICON Strategic Solutions (CDMX, home-based). Requires pharmacy/life sciences degree, supports drug safety monitoring, adverse event reporting, and regulatory compliance. Offers career development, training, and comprehensive benefits in a global FSP organization.”
“ICON Strategic Solutions seeks a remote Pharmacovigilance Project Manager in CDMX. Role involves leading drug safety projects, coordinating teams, ensuring regulatory compliance, and managing adverse event reporting. Requires scientific degree and extensive pharmacovigilance experience. Competitive salary, benefits, and career development offered.”
“ICON Strategic Solutions seeks a Project Manager for Laboratory roles in clinical trials. Requires project management experience, life sciences/healthcare background, and GCP adherence. Offers competitive salary, benefits, and career development in a sponsor-dedicated model for innovative treatments.”
“Remote Clinical Project Manager role in Brazil for ICON, leading rare diseases/CNS research projects. Requires strong project management experience, leadership, and travel (30%). Offers competitive salary, benefits, and career development in healthcare intelligence.”
“ICON seeks a Global Logistics Associate in Warsaw, Poland (hybrid role) to manage global shipping, coordinate logistics schedules, and optimize supply chain efficiency. Requires a Bachelor's degree and 1-2 years of logistics experience. Offers competitive salary, benefits, and career development opportunities.”
“Regular job offer at ICON Strategic Solutions for a Study Start Up Associate II role. Requires a Bachelor's in life sciences, 2+ years in clinical research, and regulatory affairs experience. Involves leading clinical trial initiation, ensuring compliance, and collaborating with stakeholders. Competitive benefits and career development opportunities included.”
“Remote Manager, Site Engagement role in Mexico for ICON Strategic Solutions. Requires scientific operations experience, leadership in clinical trial site engagement, and regulatory compliance. Offers competitive salary, benefits, and career development in a global FSP organization.”
“Regular job offer for a Clinical Trial Associate in Warsaw (hybrid role) at ICON Strategic Solutions. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation, and cross-functional teamwork with benefits like health coverage and learning opportunities.”
“ICON seeks a Configuration & QC Specialist I to manage clinical trial database setup (LIMS) and perform quality control checks. Requires a life sciences degree and 1+ years of relevant experience. Offers competitive salary, benefits, and career development in a collaborative healthcare research environment.”
“Full-time Clinical Research Associate (CRA II) role at ICON Strategic Solutions for Midlands-based regional travel. Requires 2+ years experience, Bachelor's in science/healthcare, and 60% travel. Competitive salary, benefits, and career growth in clinical trial monitoring.”
“Full-time Clinical Research Associate (CRA II) role at ICON Strategic Solutions. Requires 2+ years experience, scientific degree, and 60% travel. Responsible for trial monitoring, data integrity, and regulatory compliance. Competitive salary, benefits, and career development in a global FSP organization.”
“Regular job offer for a Clinical Research Associate II role at ICON Strategic Solutions. Requires 2+ years of experience, travel (~60%), and a scientific degree. Focuses on clinical trial monitoring, data integrity, and patient safety. Offers competitive salary, benefits, and career development in a collaborative environment.”
“Regular job offer for a Warehouse Coordinator in Ukraine. Requires higher education, English (upper intermediate), MS Excel skills, and logistics experience. ICON plc offers competitive salary, benefits, and career development in healthcare research logistics.”
“Regular job offer at ICON Strategic Solutions for a Study Start Up Associate I role. Requires a Bachelor's in life sciences, experience in clinical research preferred. Involves regulatory document preparation, site start-up coordination, and compliance with competitive benefits and career development opportunities.”
“Full-time Clinical Trial Manager role at ICON Strategic Solutions managing sponsor-dedicated trials. Requires medical/science degree, German/English fluency, and travel (~25%). Offers competitive salary, benefits, and career development in a global FSP organization supporting patient treatments.”
“Full-time Clinical Research Associate role at ICON Strategic Solutions, requiring 2+ years experience, German/English fluency, and 60% travel. Designs and monitors clinical trials, ensures compliance, and contributes to patient-benefiting treatments with competitive benefits and career growth.”
“Remote Clinical Research Associate II position at ICON in Spain. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career development in clinical trial monitoring for global health treatments.”
“ICON seeks a Clinical Nurse Reviewer to design, analyze clinical trials, and ensure compliance with protocols and regulations. Requires RN license, nursing experience, and travel (~10%). Offers competitive salary, benefits, and career development in healthcare research.”
“ICON seeks a Program Manager for a 2-year contract to lead laboratory facility development and expansion. Role involves end-to-end project delivery, stakeholder coordination, GMP compliance, and operational readiness. Requires engineering/life sciences degree and capital project experience in regulated environments.”
“Regulatory Scientist role at ICON plc in Bogotá, Colombia (hybrid, 3 days office). Supports regulatory submissions for clinical trials, ensures compliance with local/global regulations, and collaborates with cross-functional teams. Requires Life Sciences degree, regulatory experience, and fluency in English.”
“ICON seeks an Informed Consent Specialist I to develop, review, and approve ICFs for clinical trials, ensuring compliance with ICH/GCP and country regulations. Requires 1+ year of ICF experience, strong English skills, and stakeholder collaboration. Offers competitive salary, benefits, and career development.”
“ICON Strategic Solutions seeks a Clinical Trials Associate (CTA) to support sponsor-dedicated clinical trials. Role involves trial coordination, regulatory compliance, documentation management, and cross-functional team collaboration. Requires a scientific/healthcare degree, clinical research experience, and fluency in German and English. Competitive salary, benefits, and career development offered.”
“Remote Clinical Community Analyst role at ICON Strategic Solutions managing investigator portals for clinical trials. Requires clinical research experience and portal expertise. Offers competitive salary, benefits, and career development in a global FSP organization supporting patient treatments.”
“Remote Clinical Research Associate (CRA) II role in Mexico City for ICON Plc. Oversees site start-up, regulatory submissions, and compliance with COFEPRIS/ICh-GCP. Requires CRA experience, regulatory knowledge, and travel (~25%). Competitive salary and benefits.”
“ICON seeks a Project Manager for IDEA (Independent DMC & Endpoint Adjudication) to oversee clinical trial projects, manage budgets, and collaborate with cross-functional teams. Requires project management experience, preferably with endpoint adjudication. Offers competitive salary, benefits, and career development.”
“ICON Strategic Solutions seeks a Clinical Research Associate (CRA II) to design, monitor, and analyze clinical trials, ensuring compliance with ICH-GCP guidelines and patient safety. Requires a Bachelor's in a scientific/healthcare field, 2+ years of CRA experience, and strong organizational skills. Offers competitive salary, benefits, and career development in a collaborative, sponsor-dedicated environment.”
“ICON seeks a Lead, Clinical Trial Liaison (Lead CTL) to oversee CTL teams, provide scientific/operational support to investigator sites, and coach team members. Requires PhD/MD/PharmD, clinical research experience, and leadership skills. Competitive salary, benefits, and career development offered.”
“Remote Analytical Monitor role at ICON Strategic Solutions in Mexico. Requires 2+ years in clinical research, data analysis skills, and regulatory knowledge. Supports clinical trial oversight with data insights, risk identification, and cross-functional collaboration. Competitive benefits and inclusive workplace.”
“Full-time Clinical Research Associate (CRA II) role in Helsinki, Finland. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career growth in sponsor-dedicated clinical trial monitoring at ICON Strategic Solutions.”
“ICON seeks a CRA II for clinical trial monitoring with 2+ years experience. Role involves site visits, data integrity, protocol compliance, and collaboration. Requires travel (~60%), ICH-GCP knowledge, and scientific degree. Competitive salary and benefits included.”
“Regular job offer at ICON Strategic Solutions for a Site Activation Partner role. Requires a Bachelor's in life sciences, experience in clinical research preferred. Involves regulatory document preparation, stakeholder coordination, and travel (~5%). Competitive salary, benefits, and career development opportunities.”
“ICON is hiring a Clinical Trial Manager to oversee trial operations, ensuring compliance with regulations and timelines. Requires a science/medicine degree, monitoring experience, and 25% travel. Offers competitive salary, benefits, and career development in a global FSP organization.”
“ICON seeks a Project Manager for General Medicine to lead cross-functional teams, deliver projects on time/budget, and ensure high-quality outcomes in a global healthcare CRO environment. Requires project management experience, preferably in pharma/life sciences. Competitive salary and benefits included.”
“Lead Data Manager role at ICON Strategic Solutions for clinical trials. Requires clinical data experience, CDISC standards, and leadership skills. Competitive benefits, travel up to 15%, and focus on patient treatment development. Bachelor's degree in life sciences or related field required.”
“ICON seeks a Clinical Trial Liaison in Germany for field-based role supporting EU clinical trials. Requires MD/PharmD/PhD, clinical research experience, and strong networking skills. Role involves investigator engagement, protocol training, and recruitment strategy optimization with up to 75% travel. Competitive benefits included.”
