“Regular job offer for Sample Management Coordinator II in Assen, Netherlands. Requires MBO level 3/4 education, Dutch fluency, and 32-40h/week availability. Duties include sample registration, lab logistics, and administrative tasks. Starts with 1-year contract with potential permanent role. Market-conform salary and benefits under ICON's CAO.”
“Full-time Clinical Research Associate role at ICON Strategic Solutions. Requires scientific/healthcare degree, CRA experience, and 60% travel. Responsible for trial monitoring, data integrity, and protocol compliance. Competitive salary, benefits, and career development in a global FSP organization.”
“ICON seeks a Clinical Research Associate (CRA II) in Romania to monitor clinical trials, ensure protocol compliance, and maintain data integrity. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development.”
“ICON seeks a Clinical Trial Associate in Mexico City for office-based role. Responsibilities include trial coordination, documentation management, and cross-functional team collaboration. Requires scientific/healthcare degree and clinical research knowledge. Competitive salary, benefits, and career development offered.”
“ICON seeks a Set-Up Specialist I (Hybrid, Bulgaria) to manage clinical trial laboratory setup. Role involves coordinating client communications, ensuring compliance with protocols, and overseeing database configuration. Requires 1+ years in clinical trials, life sciences degree, and strong organizational skills. Competitive benefits package offered.”
“Regular job offer for Site Management Associate I (Regulatory) in Warsaw, Poland. Requires a Bachelor's degree in life sciences or related field, some clinical research experience preferred. Involves site monitoring, ensuring compliance with protocols and GCP guidelines, and collaborating with cross-functional teams. Offers competitive salary, benefits, and career development opportunities.”
“ICON plc seeks a Configuration & Quality Control Specialist I (Hybrid role in Bulgaria) to support clinical study setup, QC checks, and documentation. Requires a science degree, monitoring experience, and ICH-GCP knowledge. Offers competitive salary, benefits, and career development in healthcare research.”
“ICON seeks a Project Analyst I to manage supply chain, procurement, and financial tracking for clinical programs. Requires a bachelor's degree, budgeting experience, and travel up to 5%. Offers competitive salary, benefits, and career development.”
“Remote Site Management Associate II role at ICON Strategic Solutions supporting global clinical studies. Requires 1+ year in clinical trials, life science degree, eTMF/CTMS experience, and fluent English. Offers competitive salary, health benefits, and career development in a sponsor-dedicated model.”
“Full-time Clinical Trial Manager role at ICON Strategic Solutions. Requires clinical trial management experience, regulatory expertise, and travel (~25%). Offers competitive salary, benefits, and career development in a sponsor-dedicated model for innovative treatments.”
“Clinical Trial Associate role at ICON Strategic Solutions in Warsaw (hybrid). Requires a scientific degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation, and cross-functional teamwork. Offers competitive salary, benefits, and career development in a sponsor-dedicated FSP model.”
“Full-time Clinical Research Coordinator role at ICON Plc in Valencia, Spain. Requires a Bachelor's degree, extensive experience, and strong organizational skills. Manages clinical trials, ensures regulatory compliance, and supports site staff. Offers competitive salary, benefits, and career development.”
“Senior Clinical Research Associate (CRA) role at ICON Plc overseeing clinical trial monitoring, ensuring GCP compliance, site visits (60% travel), and cross-functional collaboration. Requires relevant degree and extensive CRA experience. Competitive salary, benefits, and career development in a global FSP organization.”
“Regular job offer for a Clinical Research Associate (CRA II) at ICON Strategic Solutions, a top FSP organization. Requires clinical trial monitoring experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in a sponsor-dedicated role for a top 5 pharma client.”
“Full-time Clinical Research Associate (CRA II) role at ICON Strategic Solutions. Requires 2+ years experience, scientific degree, and 60% travel. Monitors clinical trials, ensures compliance, and contributes to patient treatment advancements. Offers competitive salary, benefits, and career development in a global FSP organization.”
“Full-time Clinical Trial Associate role in Mexico City at ICON Strategic Solutions. Requires a scientific/healthcare degree, clinical research experience, and 10% travel. Offers competitive salary, benefits, and career development in a global FSP organization supporting patient treatments.”
“ICON seeks a Program Manager for Biotech projects with therapy area experience in Respiratory, Ophthalmology, or Immunology. Role involves leading cross-functional teams, managing budgets, timelines, and delivering complex programs. Requires strong leadership, PMP certification preferred, and 25% travel. Competitive salary, benefits, and career development offered.”
“Regular Clinical Scientist role at ICON Strategic Solutions requiring Veeva EDC experience and clinical research background. Offers competitive salary, benefits, and remote work (#LI-Remote). Focus on clinical trial design, data analysis, and cross-functional collaboration.”
“ICON seeks a Program Manager to lead complex healthcare projects, ensuring timely delivery within budget and scope. Requires strong leadership, PMP certification (preferred), and 25% travel. Offers competitive salary, benefits, and career growth in a global clinical research organization.”
“Regular job offer for Site Management Associate I in Greater Sao Paulo Area (Office with Flex). Supports clinical trial site management, ensures protocol compliance, and maintains operational efficiency. Requires relevant degree, English proficiency, and clinical research experience. Competitive benefits and career development opportunities included.”
“Clinical Trial Manager role at ICON Strategic Solutions overseeing trial design, data analysis, and regulatory compliance. Requires clinical trial experience, travel (~25%), and a relevant degree. Offers competitive salary, benefits, and career development in a global FSP organization.”
“Full-time Associate Statistical Programmer role in Bengaluru for ICON Strategic Solutions. Requires 0-2 years experience in R and SAS programming for clinical research. Responsibilities include creating statistical programs, validating outputs, and adhering to project timelines. Competitive salary, benefits, and career development opportunities.”
“Regular job offer for a Lab Analyst I position in ICON's QC laboratory in Assen, Netherlands. Requires MLO/HLO education, GMP knowledge, and 32-40h/week availability. Involves HPLC/UPLC, KF analysis, and GMP environment work with potential permanent contract after 1 year.”
“Regular job offer for a Site Engagement Lead at ICON Strategic Solutions. Requires life sciences degree, clinical research experience, and 60% travel. Competitive salary, benefits, and career development in clinical trial site management.”
“Talent Acquisition Business Partner role in Mexico City (hybrid) at ICON, a healthcare research firm. Requires HR experience, strategic recruitment skills, and English proficiency. Offers competitive salary, benefits, and career development in a DEI-focused environment.”
“Regular job offer for a Study Start Up Associate II role at ICON Strategic Solutions, requiring 2+ years in clinical research or regulatory affairs. Involves leading clinical trial initiation, regulatory submissions, and stakeholder coordination. Competitive benefits and career development opportunities included.”
“ICON seeks an experienced EUC Manager in Dublin for a hybrid role (60% office) to lead end-user computing teams, manage Citrix, Intune, SCCM, and virtual desktops, ensuring secure and reliable IT operations with strong leadership and technical expertise.”
“ICON Strategic Solutions seeks a Payment Analyst (Investigator Payment Associate) to process investigator payments, ensure regulatory compliance, and support financial aspects of clinical trials. Requires finance/accounting experience, proficiency in Excel/SAP, and knowledge of Sunshine Act/FMV. Offers competitive salary, benefits, and career development in a collaborative pharmaceutical FSP environment.”
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|Graduate Programme, Medizin, Englisch
“Graduate Pharmacovigilance Associate role at ICON Strategic Solutions (home-based in Mexico). Requires a Bachelor's in pharmacy/life sciences, supports adverse event data collection, safety reporting, and regulatory compliance. Offers competitive salary, benefits, training, and career development in drug safety monitoring.”
“ICON seeks a Clinical Site Associate to support site management in clinical trials, handling document tracking, site communications, and compliance. Requires a life sciences/healthcare degree or equivalent experience, strong organizational skills, and occasional travel (10%). Office-based role with 3 days on-site.”
“Remote role for ICON Strategic Solutions as a Site Management Associate supporting global clinical studies. Requires 1+ years in clinical trials, life science degree, and eTMF/CTMS experience. Competitive salary, health benefits, and career development in a sponsor-dedicated FSP model.”
“Regular job offer for a Site Engagement Lead at ICON Strategic Solutions. Requires clinical research experience, travel (~60%), and life sciences degree. Competitive salary, benefits, and career development in clinical trial site management.”
“Clinical Trial Administrator role at ICON in Sofia, Bulgaria (hybrid). Requires scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation, and cross-functional teamwork. Offers competitive salary, benefits, and career development in a sponsor-dedicated model.”
“ICON Strategic Solutions seeks a Biosampling Project Manager to oversee biosample and laboratory strategies for clinical studies. Role involves managing vendors, ensuring sample quality, and collaborating with stakeholders. Requires clinical trial experience, GxP knowledge, and regulatory compliance skills. Competitive benefits and remote work available.”
“Full-time Clinical Trial Associate (CTA I) role in Sofia, Bulgaria, at ICON Strategic Solutions. Hybrid work model. Requires a Bachelor's in a scientific/healthcare field, clinical research experience, and knowledge of trial regulations. Competitive salary, benefits, and career development in FSP organization.”
“ICON seeks a Manager, Clinical Operations in Hungary to oversee clinical trial execution, ensure regulatory compliance, lead teams, and optimize processes. Requires scientific degree, extensive experience, and 30% travel. Competitive salary and benefits included.”
“ICON seeks a Clinical Research Associate (CRA II) to design, monitor, and analyze clinical trials, ensuring compliance, data integrity, and patient safety. Requires 2+ years of experience, a scientific degree, and 60% travel. Competitive benefits and inclusive workplace offered.”
“ICON is hiring a Contract Analyst II for home-based UK role. Responsibilities include contract management, negotiation, and analysis for clinical trials. Requires 2+ years in contract management, preferably in pharma/clinical research. Competitive salary, benefits, and career development offered.”
“Clinical Research Coordinator I role at ICON for designing and analyzing clinical trials, data interpretation, and trial coordination. Requires life sciences degree or relevant experience, organizational skills, and proficiency in Microsoft Office. Competitive salary and benefits package offered.”
“ICON seeks a German-speaking Site Contracts Negotiator II (remote) in Hungary to manage clinical trial agreements, budgets, and negotiations with investigator sites. Requires legal/business background, fluency in German/Hungarian/English, and contract management experience. Offers competitive salary, benefits, and career development in healthcare research.”
“Regular job offer for a Clinical Research Associate I (CRA I) in Guatemala. Requires a medical/science degree, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career development opportunities at ICON, a global healthcare research organization.”
“CRA II role at ICON Strategic Solutions for clinical trial monitoring, requiring 2+ years experience, 60% travel, and ICH-GCP knowledge. Offers competitive salary, benefits, and career development in a sponsor-dedicated model for global clinical trials.”
“Regular job offer at ICON Strategic Solutions for a Study Start Up Associate I role. Requires a Bachelor's degree in life sciences, experience in clinical research preferred, and involves facilitating clinical trial initiation, regulatory compliance, and stakeholder coordination. Competitive salary and benefits package offered.”
“Regular job offer at ICON Strategic Solutions for a Site Engagement Liaison role in clinical research. Requires life sciences degree, clinical experience, and dermatology background. Salary up to EUR 68,120 with benefits. 60% travel required. Full-time position.”
“Regular job offer for Contract Analyst II at ICON Strategic Solutions. Requires 2+ years in contract management, preferably in pharma/clinical research. Salary range EUR 37,224–46,530. Focus on clinical trial contracts, negotiation, and compliance. Full benefits, travel 5%.”
“Remote Clinical Data Risk Analyst role at ICON Strategic Solutions, Argentina. Conducts risk assessments on clinical trial data, collaborates with cross-functional teams, and ensures data integrity and regulatory compliance. Requires degree in statistics/life sciences and clinical data analysis experience. Offers competitive salary, benefits, and career development.”
“ICON seeks an Informed Consent Specialist II to lead development and review of global clinical trial consent documents, ensuring regulatory compliance and patient-friendly language. Requires clinical research experience, GCP knowledge, and stakeholder management skills. Offers competitive benefits and career growth.”
“ICON seeks a Pharmacovigilance Associate to monitor pharmaceutical safety, collect adverse event reports, conduct risk assessments, and ensure regulatory compliance. Requires a relevant degree and experience in pharmacovigilance/drug safety. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
“ICON seeks a Clinical Data Coordinator II for Mexico and Colombia to manage clinical trials, interpret medical data, and ensure data accuracy using systems like Medidata. Requires a relevant degree, intermediate clinical data experience, and strong communication skills. Hybrid role with competitive benefits and career development opportunities.”
“ICON seeks a Site Specialist to manage site support activities, coordinate documentation, and ensure clinical trial compliance. Requires a Bachelor's in life sciences/healthcare, relevant experience, and strong organizational skills. Competitive salary, benefits, and career development offered.”
