site activation

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Job SummaryJoin Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

Pasantía Country Site Activation - CABA, ArgentinaPart time, morning, Hybrid - 4 days OB - 1 day HBEssential Functions:•    Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Local Teams and other departments...

Worldwide Clinical Trials in Argentina seeks a subject matter expert and local point of contact for regulatory submissions, site activation, and maintenance for awarded projects. You will plan, initiate, and track documents required for regulatory submissions, and ensure country requirements are met to achieve site activation goals.You will coordinate with...

Pasantía Country Site Activation - CABA, Argentina Part time, morning, Hybrid - 4 days OB - 1 day HB Essential Functions: • Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Local Teams and other departments...

Site Activation Specialist (US Experience)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 outcomes to address modern market realities.  Every day we perform better because of how we work together, as one...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global...

Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory...

Description Site Activation Specialist (US Experience) 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 outcomes to address modern market realities. Every day we perform better because of how we work...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global...

Medpace in Buenos Aires is seeking a Regulatory Submissions Coordinator to join our Regulatory Submissions team. You will work on multiple projects and gain experience in regulatory processes while being mentored and supported for career development.You will collaborate with Coordinators to collect essential documents, prepare submissions, and ensure...

Job Overview Full time - Hybird role (CABA, Argentina) The Site Activation Coordinator will give support to Argentina in tasks related to import/export activities for site activation. Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations,...

Job OverviewLead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regions. This role is responsible for accelerating site activation to support timely patient enrollment, including Site Identification and Selection, Ethics and Regulatory submissions, and Site Contracting in line with...

Mastercard is expanding its Services Customer Success team in the LATAM region. The Regional Customer Success Manager will work with cross‑functional teams to drive customer engagement, grow the business, and ensure readiness of technical programs for priority customers in Argentina and Brazil.The role emphasizes translating complex capabilities into clear...

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory and start-up activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors; maintains,...

Farmacias-Central-Oeste is seeking an experienced Senior Clinical Site Activation professional to lead activation and maintenance of clinical studies. You will coordinate with Regulatory, QA, and cross-functional teams to ensure compliant and timely study startup and ongoing maintenance.The role requires strong negotiation, excellent communication and...

Syneos Health is seeking a Global Site Activation Manager for LATAM to lead Site Start-Up activities with global scope. The role requires 3–4 years of experience as a site activation lead in a CRO environment, delivering activation-ready sites on time and within budget.Responsibilities include coordinating with cross-functional teams, ensuring regulatory...

IQVIA, a leading global provider of clinical research services and healthcare insights, is seeking a junior candidate for site activation activities. You will act as SPOC for feasibility and activation of investigative sites and collaborate with SAM, PM, and other departments to ensure timely contract and document execution.The role requires a life sciences...

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. What You Will Do Your role will involve delivering site start-up and activation work to a high...