Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Leads patient-centric medical writing projects with a primary focus on Informed Consent Forms (ICFs) through collaboration with internal and client teams. Manages project timelines, budgets, and resources. Manages and ensures
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior ICF Medical Writing Project Manager (PM) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Who we are We’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
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Study Start-Up Associate II (FSP - Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity,
Descrição da empresa A QIMA Life Sciences (ICF) é uma divisão de rápido crescimento do Grupo QIMA, dedicada a fornecer serviços completos para a indústria de ciências da vida – desde P&D até o lançamento no mercado.
About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research
Under moderate supervision, the Regulatory and Start Up Specialist 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
Job Overview Under general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation The Senior Medical Writer provides high-quality medical and scientific writing from planning and
About NIIT NIIT provides comprehensive and scalable managed training services for learning administration that maps directly to our customer needs. Training is our business and passion. We are one of the largest training outsourcing providers in
Crinetics is a pharmaceutical company headquartered in San Diego, California, with a growing presence in Latin America, including an office in Brazil. We are developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We
Our Site Activation Specialists work under moderate supervision, executing the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. You will prepare and
You will be a practitioner on our telehealth platform Intellect, where your role is to support our clients mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled
Assistente Técnico Responsável por reparo e manutenção de aparelhos eletrônicos (TV, celular e similares), diagnóstico de falhas, substituição de peças e suporte técnico. Necessário possuir CNH válida para deslocamentos externos. Não é necessário ter experiência, oferecemos
In short Position: Junior Clinical Development Location: Azuqueca de Henares. Experience: 3 to 5 years in similar roles. Want to know more? NSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and expertise
Study Start-Up Associate II (FSP - Sponsor Dedicated) 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
When our values align, theres no limit to what we can achieve. An initiation Clinical Research Associate (i CRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the