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
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
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,
Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety. We have a vacancy for a Senior ICF Medical Writing Project Manager based in Mexico. Discover
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
Job Description Under moderate supervision, the Site Activation 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
In short Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. Position: Junior Clinical Development Location: Azuqueca de Henares. Experience: 3
Senior Clinical Trial Manager Senior Clinical Trial Manager responsible for the execution of Phase I‑IV clinical studies at the country level, ensuring end‑to‑end study operational oversight and delivery, adherence to timelines, budget and quality standards. Position
In short Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. Position: Junior Clinical Development Location: Azuqueca de Henares. Experience: 3 to 5 years in similar roles. Want
Under moderate supervision, the Site Activation 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 site documentation;
Job Overview Under general supervision, perform tasks at a country level associated with contracts for site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May
# Senior Clinical Trial ManagerSão Paulo - SP - BRFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working
# Sr. Site Activation Specialist in BrazilApplylocations: São Paulo, Braziltime type: Full timeposted on: Posted Yesterdayjob requisition id: R Under moderate supervision, the Sr . Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and
# Site Activation Specialist in BrazilApplylocations: São Paulo, Braziltime type: Full timeposted on: Posted Yesterdayjob requisition id: R Internal Job DescriptionUnder moderate supervision, the Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and maintenance
Under moderate supervision, the Sr . Site Activation 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
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
Job Overview Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point