Project analyst i 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 project analyst i to join our diverse and dynamic team. working closely with our project team, you will provide invaluable guidance and support, ensuring that every task is accomplished with precision and efficiency. you will have the opportunity to collaborate with diverse stakeholders, including clients and vendors, to achieve project objectives and deliverables. your responsibilities: recognizing, exemplifying and adhering to icon's values which centers around our commitment to people, clients and performance. embracing and contributing to a culture of continuous process improvement, streamlining workflows, adding value, and meeting client needs. acting as a key point of contact for assigned clients, gathering project requirements, ensuring smooth project initiation, and managing expectations throughout the project lifecycle. independently managing small to mid-sized translation projects, ensuring alignment with client expectations, timelines, budgets, and quality standards. defining project tasks, monitor progress, track milestones, and proactively managing risks, escalating when necessary. coordinating effectively with internal teams to ensure seamless execution and communication. contributing to internal and client-facing reporting, performance tracking, and issue resol...
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. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed...
Desktop publishing specialist - language services - homebased - colombia and brazil (only) 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 desktop publishing specialist - language services to join our diverse and dynamic team. the desktop publishing specialist in icon language services provides project preparation and dtp assistance to translation project managers. what you will be doing: - preparation of project files as needed, which may include: - file conversion and formatting from one file format to another (ex. from pdf to word).- recreation of dead text in source documents.- other source formatting adjustments as requested by clients to prepare the files for cat tool import.- file alignments in the cat tool.- other quality control tasks, as needed.- review and correct the layout of translated documents that are exported from the cat tool.- troubleshoot document formatting issues as needed. coordinate and communicate with project managers in a professional and timely manner.- provide input and suggestions towards innovating new approaches and product features tailored to team formatting needs.- ensure client satisfaction with formatting on all projects under his/her responsibility your profile: - associates degree in appropriate field of study, preferably in graphic design or similar field.- 2+ years of word processing/d...
Cta - colombia, bogota 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 our diverse and dynamic team. as a clinical trial administrator at icon, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innvative treatments and therapies. what you will be doing - assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. - maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. - support the preparation of study-related materials, such as informed consent forms and case report forms. - work with cross-functional teams to facilitate communication and ensure smooth trial execution. - contribute to the tracking and reporting of clinical trial metrics and milestones. **profile**: - bachelor's degree in a scientific or healthcare-related field. - prior experience or strong interest in clinical research. - knwledge of clinical trial processes, regulations, and guidelines. - excellent organizational and communication skills. - ability to work collaboratively in a fast-paced environment with attention to detail. what icon can offer you: - our succes...
Job title: pharmacovigilance associate job location: bogotá, bogota, colombia job location type: on-site job contract type: permanent job seniority level: home based 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 pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clini...
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