“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 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.”
“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 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.”
“ICON seeks a Manager for Patient Recruitment in Coventry, UK. Role involves leading recruitment strategies for clinical trials in EMEA, managing teams, and ensuring study objectives are met. Requires Life Sciences degree and experience in patient recruitment within CROs or pharma. Competitive salary and benefits offered.”
“Lead Medical Writer role at ICON Strategic Solutions for clinical research projects. Requires medical writing expertise, regulatory knowledge, and team leadership. Offers competitive salary, benefits, and career development in a global FSP organization contributing to patient treatments.”
“ICON seeks a Clinical Trial Liaison in Czech Republic for field-based role supporting EU trials. Requires MD/PharmD/PhD, clinical research experience, and strong networking skills. 75% travel, home/office-based. Competitive salary and benefits included.”
“ICON seeks a Medical Admin Assistant to support clinical trials with executive administration, documentation management, and regulatory coordination. Requires administrative experience, preferably in healthcare, with strong organizational and communication skills. Competitive salary and benefits package offered.”
“ICON seeks a Clinical Trial Liaison in Italy for field-based role supporting European trials. Requires MD/PharmD/PhD, clinical research experience, and strong EU network. 75% travel, competitive salary (€54k-€68k), benefits, and home/office-based work. English and Italian proficiency required.”
“ICON seeks a field-based Clinical Trial Liaison in Turkey to support clinical trials across Europe. Role involves engaging investigators, providing scientific guidance, and improving patient enrolment. Requires MD/PharmD/PhD, clinical research experience, and strong networking skills. Home- or office-based with 75% travel. Competitive salary and benefits included.”
“ICON seeks a Clinical Trial Liaison in France for field-based role supporting clinical trials across Europe. Requires MD/PharmD/PhD, clinical research experience, and strong scientific network. Role involves investigator engagement, recruitment strategies, and protocol training. Competitive benefits and travel up to 75% included.”
“ICON seeks a Supervisor for Accounts Payable to manage invoice processing, corporate credit card administration, and team workflows. Requires finance/accounting degree, leadership experience, and knowledge of Oracle/ServiceNow. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
“Scientific Affairs Specialist I role at ICON in Mexico City (remote) for a global healthcare CRO. 2+ years experience required in scientific affairs, central lab services, or diagnostics. Duties include assay configuration, scientific communication, client engagement, and troubleshooting. Benefits include competitive salary, health coverage, and learning opportunities.”
“Regular job offer for Study Start Up Associate I in Argentina at ICON Strategic Solutions. Requires life sciences degree, clinical research experience preferred. Focuses on clinical trial initiation, regulatory compliance, and stakeholder coordination. Competitive benefits and career development included.”
“Senior Clinical Research Associate (CRA II) role at ICON Strategic Solutions for clinical trial monitoring, requiring 2+ years experience, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career development in a sponsor-dedicated model for innovative treatments.”
“ICON Strategic Solutions seeks a Grants Specialist to manage grant applications, research opportunities, ensure compliance, and collaborate on clinical programmes. Requires a Bachelor's degree, grant writing experience, and strong communication skills. Offers competitive salary, benefits, and career development in a global FSP organization.”
“Regular job offer for Study Start Up Associate II at ICON Strategic Solutions. Requires 2+ years in clinical research/regulatory affairs, Bachelor's in life sciences, and travel up to 5%. Competitive salary, benefits, and career development in sponsor-dedicated model for clinical trial initiation.”
“ICON seeks a CRA II/Senior CRA for Early Phase clinical trials in the UK. Role involves site management, patient safety oversight, and data integrity. Requires ICH-GCP knowledge, travel, and healthcare degree. Competitive salary and benefits offered.”
“Senior Clinical Research Associate (CRA II) role at ICON Strategic Solutions in São Paulo or Porto Alegre. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career development in clinical trial monitoring and patient-focused drug development.”
“Office-based (hybrid after 4 months) role in Mexico City for ICON Strategic Solutions as Site Management Associate II. Requires 2+ years in clinical research, TMF management, and GCP compliance. Competitive salary, benefits, and career development in clinical trials.”
“ICON seeks a Contract Analyst II for Early Phase studies in Sofia, Bulgaria or UK. Hybrid role requiring 2+ years in sponsor contract management, financial analysis, and budgeting. Competitive salary, benefits, and career development opportunities in healthcare intelligence and clinical research.”
“ICON seeks a Product Manager for ServiceNow in Dublin, Ireland. Hybrid role requiring 3+ years in Product Management or Platform Ownership, preferably with ServiceNow certifications. Responsibilities include strategy, stakeholder management, governance, and financial oversight. Offers competitive salary, benefits, and career development opportunities.”
“Medical Research Associate role at ICON for clinical drug research. Requires BIG registration, MBO level education, and verpleegtechnische skills. Involves data collection, participant monitoring, and protocol adherence. Competitive salary, benefits, and career development included.”
“Medical Research Associate role at ICON, a global clinical research organization. Responsible for executing nursing tasks, collecting research data, and ensuring participant safety in pharmaceutical studies. Requires BIG registration and experience in clinical research. Competitive salary and benefits package offered.”
“Clinical Research Associate II role at ICON in Groningen, Netherlands. Hybrid or remote position requiring clinical monitoring experience, ICH-GCP knowledge, and strong communication skills. Involves site management, data integrity, and regulatory compliance for early-phase clinical trials.”
“ICON seeks an IHCRA to manage clinical trials, ensuring compliance with GCP, site payments, and contract negotiations. Requires experience in clinical study coordination, VeeVa Systems, and regulatory knowledge. Competitive salary, benefits, and career development offered.”
“ICON seeks a Clinical Research Associate II (CRA II) in Paris or Lyon for Phase I-III trial monitoring. Requires French residency, advanced life sciences degree, and CRA experience. Hybrid/remote role with oncology, neurology, and other therapeutic areas. Competitive benefits and inclusive workplace.”
“Full-time Clinical Data Coordinator II role at ICON, a global clinical research organization. Requires a relevant bachelor's degree, clinical data management experience, and familiarity with data systems like Medidata. Involves designing trials, ensuring data quality, collaborating with teams, and mentoring junior staff. Offers competitive salary, benefits, and travel (5%).”
“ICON seeks a Clinical Trial Manager for Real World Evidence (RWE) roles in Bulgaria, Georgia, Poland, or South Africa. Requires 2+ years in clinical trial management, RWE exposure, and ability to manage teams. Competitive salary, benefits, and travel (15%) included. Remote work eligible (#LI - Remote).”
“ICON seeks a Pharmacovigilance Reporting Associate to prepare safety reports for clinical trials and post-marketing activities. Requires life sciences/pharmacy degree, pharmacovigilance experience, and regulatory knowledge. Offers hybrid work, competitive salary, and comprehensive benefits including health coverage and career development.”
“ICON seeks a Clinical Research Associate (CRA II) with 2+ years experience to monitor clinical trials, ensure protocol compliance, and maintain data integrity. Role involves site visits, collaboration with investigators, and travel (~60%). Competitive salary, benefits, and career development offered.”
“ICON seeks an Account Development Manager to drive business growth in clinical research. Role involves relationship-building, lead generation, and strategic account management for pharmaceutical/biotech clients. Competitive salary, benefits, and career progression in a global CRO. Ideal for commercial professionals with healthcare experience.”
