Site Specialist I

hace 6 días


Buenos Aires, Argentina Brainlabs A tiempo completo

Site Specialist IICON plc Site Specialist IICON 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. Responsibilities Proficient knowledge of ICON SOPs/WPs, ICH/GCP and applicable country regulations/guidelines and ICON systems. Support Site Partners to collect, review, organize and assemble initial start‑up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities, any other local regulatory authorities as required by countries and in accordance with ICH/GCP and applicable country regulations/guidelines. Support collection and assembling of all documents needed in the Critical Document Package (CDP) and/or those required for site activation, ensuring that Sponsor and Investigator obligations are being met and are in compliance with applicable requirements and ICH/GCP guidelines. Support coordination of all necessary translations required for any start‑up documentation. Perform timely and accurate progress data entry of all documents collected from sites and of the relevant study site activation activities into the appropriate tracking systems and tools. Participate to internal study review meetings with study teams to provide updates on site progress in document collection and on the executed site activation tasks. Accurately forecast Site Activation plans and ensure that they are reflected accurately in ICON’s systems and proactively follow through for achievement to plan. Ensure accuracy and timely completeness of Trial Master File (TMF) documents submitted during start‑up and perform a Quality Control (QC) review of files before transfer to maintenance for filing in TMF. Attend study team meetings as required. What you need to succeed in the role Bachelor’s Degree preferably in Life Sciences. Minimum of 1 year’s experience or understanding of clinical study start‑up requirements and activities. Knowledge of local and/or international regulatory processes, including submissions to regulatory authorities and ethics committees. Ability to read and understand clinical protocols, regulatory documents, and study‑specific processes. Strong attention to detail and organizational skills. Ability to work independently and manage multiple tasks simultaneously in a fast‑paced environment. Excellent communication skills both in English and Spanish. 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’s well‑being. 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, TELUS Health, offering 24‑hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others. LI‑FP1LI‑Hybrid Visit ourcareers site to read more about the benefits ICON offers. Clinical Site Technology Specialist PSI CRO Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on... Syneos - Clinical and Corporate - Prod Description Sr IMS Specialist (Site Payments) - Buenos Aires ARG Hybrid Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into... Site Reliability Engineer Observability Lead Unilever Responsibilities Create a robust observability framework, including an APM, alarming, dashboarding, event correlation, integrated to an existing observability platform. Perform analytics on previous incidents and usage... Cra I, Cra II or Senior Cra, Single‑sponsor ICON Plc CRA I, CRA II, Sr. CRA - Chile, Santiago 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 ... Cra (Level I) PPD JOB DESCRIPTION: PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in‑between, it’s you We know that meaningful results not only require the right approach, but also the right people. We invite you to re‑imagine health... Cra (Level I) Thermo Fisher Scientific PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in‑between, it’s you We know that meaningful results not only require the right approach, but also the right people. We invite you to re‑imagine health promoting protocols... Site Merchandising and Ecom Support Global Fidelis We are currently looking for a Website Merchandising and Ecom Support specialist. Creating and managing items and outfits on site. Upload Marketing creative assets to site. Assist in promotion tool and pricing set‑up and troubleshooting. Assist with Site navigation... Article 6 Readiness Specialist Consultant for Argentina - Capacity Building in Carbon Markets a… myGwork - LGBTQ+ Business Community This job is with United Nations, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Result of Service The Article 6 Readiness Specialist Consultant for Argentina will… Account Executive I Xometry Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry’s digital marketplace gives manufacturers the critical resources they need to grow their business while also… Attorney Specialist - Commercial Contracts Ecolab Inc. The Ecolab GBS+ Buenos Aires Attorney Specialist - Commercial Contracts position will start by assisting with the review and creation of commercial contracts for our North American business. In addition to helping… Internal Comms Specialist Greenpeace Permanent* / full time Greenpeace is a story of ordinary people doing extraordinary things. It’s a story of people who believe in hope in action because a billion acts of courage can change the world. 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