Job Description #ONEGDMS Position Overview Under the direction of the Director/Associate Director, the Lead CDT Analyst creates and executes Quality Control (QC) testing and User Acceptance Testing (UAT) procedures for electronic data capture (EDC) systems. This
Description The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and
Node.js Developer What Youll Bring to The Team: We are seeking talented Node.js developers to contribute to the development of new products for our client. You will work on cutting-edge solutions that support clinical trials and drive innovation
Job Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a customer or a specific program for a customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up
Job Overview Under direct supervision, sets up studies and data integrations within sample tracking software systems, interfacing with internal and external stakeholders. Trains and assists end users with system usage. Performs system configuration and/or testing of
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
DevOps Engineer What Youll Bring to The Team: We are looking for a talented DevOps Engineer to build the infrastructure that will enable the future of clinical trials, contributing to the development of new products for our client.
Overview ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at
Company Description Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. Please submit
Date Posted:2025-03-10 Country:United States of America Location:Villages-Buenos Aires WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive
Date Posted:2025-03-13 Country:United States of America Location:Villages-Buenos Aires WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description 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 ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Job Description The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description About the Role Monitors investigator sites with a risk-based monitoring approach, applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions
Work Schedule Environmental Conditions Job Description Summarized Purpose: Provides complete oversight of supply chain for sophisticated global clinical trials. Ensures project/study activities are in compliance with company and client requirements. Acts as a representative for the department on
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description *Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Coordinating multiple complex projects from initiation through delivery, ensuring they meet scope, quality, time, and cost constraints. Key Responsibilities Lead Projects: Manage and monitor multiple related projects, ensuring they
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description 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 customers to
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Summarized Purpose: Provides complete oversight of vendor supply chain for moderate complexity clinical trials in single or more than one region. Selects and contracts with appropriate vendors for scope of clients
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