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
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.
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
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
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 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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Completes study and site management activities as defined in task matrix, and as applicable to study assigned. Completes and documents study-specific training. Orients and trains on any CRG/study-specific
Work ScheduleOther 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
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical
Job Title: Executive Assistant Location: Remote UK (British time) Salary Range: up to 1500 USD Work Schedule: Monday - Friday, 10:00 AM to 6:00 PM (BST) NOTE: INDEPENDENT CONTRACTOR POSITION Company Overview: Sagan is an exclusive
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 clinical
