Clinical Trial Associate
hace 21 horas
Overview ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. This role is Mexico-based and office-based. Responsibilities Data entry and data management of CTMS ICF tracking and reconciliation Document management including essential document filing and TMF reconciliation Support vendor management: compile meeting agendas, minutes; reconcile vendor reports; assist with coordinating delivery of materials for SIV Investigator meeting support, assist in meeting planning, drafting and finalizing agenda, attendee expense reports Coordinate site equipment provisioning Coordinate investigator brochure translation, printing and distribution Knowledge Proficient in the use of computer and software such as MS WORD, Excel, Power Point, etc. Good verbal and written communication skills (English and regional) Attention to detail and ability to multi-task Good organizational, record retention and time management skills Key competencies Attention to detail Delivery focus Team work Time management Policy, process and procedural conformance Basic qualifications Associate’s degree or higher education Preferred qualifications 3 years work experience in life sciences, or medically related field What ICON can offer you Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site ( to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here ( to apply #J-18808-Ljbffr
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Clinical Trial Associate
hace 6 días
distrito federal, México ICON A tiempo completoClinical Trial Associate, Shanghai, office base ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial...
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Clinical Trial Associate
hace 4 semanas
distrito federal, México ICON A tiempo completoCTA-Partial Home Base-South Korea ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial Administrator to join...
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Remote Clinical Trial Delivery Manager
hace 2 días
distrito federal, México ICON Clinical Research A tiempo completoA leading clinical research organization is seeking a Clinical Trial Manager based in Mexico. The successful candidate will oversee the planning, execution, and completion of clinical trials, ensuring adherence to standards and compliance with regulations. Collaborating with cross-functional teams and managing site relationships is key to this role....
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Shanghai Clinical Trial Associate-Coordination
hace 6 días
distrito federal, México ICON A tiempo completoA global clinical research organization is seeking a Clinical Trial Administrator in Mexico City. In this role, you will assist with the coordination and administration of clinical trials, maintain documentation, and contribute to study preparation. Ideal candidates have a Bachelor's degree in a relevant field and strong communication skills, with an...
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Clinical Trial Operations Coordinator
hace 21 horas
distrito federal, México ICON Clinical Research A tiempo completoA leading clinical research organization based in Mexico City seeks candidates for a role focused on data management and support for clinical trials. The successful applicant will perform tasks such as data entry, document management, and vendor support, requiring attention to detail and strong organizational skills. Candidates should have an Associate’s...
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Clinical Trial Delivery Lead
hace 3 días
distrito federal, México ICON Strategic Solutions A tiempo completoA global clinical research organization is seeking a Study Delivery Manager in Mexico City to oversee clinical trials' planning and execution. This role requires excellent collaboration with cross-functional teams and strong relationships with stakeholders. Candidates should have a university degree in a relevant field and significant experience in clinical...
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Remote Senior Clinical Supply Operations Lead CDMX
hace 4 semanas
distrito federal, México ICON A tiempo completoA leading healthcare organization in Mexico City is seeking a Senior Clinical Supply Associate to manage clinical trial supplies. The role involves planning, logistics, and ensuring compliance with regulatory standards. Ideal candidates will have significant experience in clinical supply chain management and an advanced degree in a relevant field. We offer...
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Assoc Clinical Lead
hace 2 días
distrito federal, México IQVIA A tiempo completoJob Overview Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance...
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Clinical Trial Nurse Monterrey, Nuevo Leon, Mexico
hace 3 semanas
distrito federal, México IQVIA A tiempo completoClinical Trial Nurse Per Diem Work Set-Up: Local Travel In-Home Patient Visits Are you a Registered Nurse looking for a flexible and rewarding opportunity in clinical research. Join IQVIA, a global leader in advancing healthcare, and make a real impact by supporting clinical trials in your community. We’re seeking experienced Registered Nurses to visit...
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Part-Time In-Home Clinical Trial Nurse
hace 3 semanas
distrito federal, México IQVIA A tiempo completoA leading global healthcare firm is seeking a Clinical Trial Nurse Per Diem for home visits in Mexico City. This part-time position requires an active RN license and BLS certification, with responsibilities including in-home patient visits, sample collection, and data documentation. Enjoy a flexible schedule ideal for PRN nurses and gain valuable experience...
