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C-Clinical Dallas jobs
Clinical Research Associate - Vancouver, Canada We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in desig...
Sr Trial Delivery Manager As a Trial Delivery Management (Advanced) at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives. What You Will Do: Yo...
Feasibility Principal Analyst - Home-Based (US) Reporting to the Director of Feasibility, the Feasibility Principal provides strategic, study-level feasibility leadership within the Patient and Site Engagement (PSE) team...
Data Engineer/Architect We are seeking a Data Engineer / Architect to support the design and delivery of a modern, scalable data foundation. The role focuses on building robust, automated data architectures that bring to...
Trial Delivery Management (Advanced) As a Trial Delivery Manager (Advanced) at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives. What You Wil...
Manager of Study Start Up As a Manager, Study Start Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulato...
Supplier Performance Monitor Key Responsibilities: Monitoring the collection, processing, and analysis of data from external third-party Supplier for sponsored clinical trials Monitoring and evaluating Supplier complianc...
Clinical Trial Transparency Specialist As a Clinical Trial Transparency Associate at ICON, you will be responsible for processing the anonymization of clinical trial documents and datasets required for public disclosure....
RSTM/eCOA Manager As a RTSM/eCOA Manager, you will be responsible for end-to-end leadership of Randomization and Trial Supply Management (RTSM/IRT) systems and eCOA in collaboration with Clinical Operations across a dive...
Lead CRA - Ophthalmology We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical tri...
Sr CRA - Ophthalmology As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will...
Medical Director We are seeking an experienced Medical Director to play a critical role in supporting patient safety throughout the lifecycle of ICON’s innovative therapies. In this position, you will drive medical safet...
Senior Clinical Research Associate - Oncology Early Development - Toronto The Sr. Clinical Research Associate (Sr. CRA) willbe responsible forperforming investigative site management and monitoring activities throughout...
CRA II - NOVO Calgary As a CRA II (Client Dedicated) at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What...
Investigator Payments - Disease Area Lead As a Supervisor, Investigator Payments at ICON, you will manage and oversee the processing and tracking of investigator payments, ensuring timely and accurate payments in complia...
Project Manager (Study Start Up) - Canada The Start Up Project Manager (SUPM) is responsible for defining, developing and delivering the global study start up project strategy by partnering with roles across GSSO, CD&...
Lead Medical Writer As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments a...
RWE Scientist As an RWE Scientist at ICON, you will lead the development, validation, and management of clinical databases and data systems, ensuring high-quality data outputs for clinical trials. What You Will Do: Strat...
Senior Clinical Research Associate - Oncology - West Coast As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, a...
Senior Clinical Trial Manager Oncology As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our c...
Manager, Medical Writing As a Manager, Medical Writing at ICON, you will lead a team of medical writers to produce high-quality, scientifically accurate documents in support of clinical trials. What You Will Do: Your foc...
Study Start Up Manager As a Manager, Study Start Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory...
Sr. Manager, Clinical Compliance As a Senior Manager, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of i...
Third Party Quality Lead - US or Canada The Third Party Quality Lead (TPQL) reports to the Head of Third Party Quality and partners with stakeholders to manage third-party quality risk, issue resolution, and GCP complian...
Global Contracts Analyst As a Global Contract Analyst at ICON, you will manage contractual agreements, ensuring compliance, and contribute to the advancement of innovative treatments and therapies. What You Will Do: Your...
Quality ICM Issue Lead - US or Canada The Issue Lead will be responsible for driving QE case management, ensuring that investigations are conducted thoroughly within timelines and compliance requirements, overseeing the...
Quality ICM Senior Issue Lead - US or Canada The Senior Issue Lead will be accountable for Quality Events: managing confirmed Major / Critical Quality Event (QE) cases through the investigation process including root cau...
Drug Development Project Manager - Boston The Drug Development Project Manager oversees the high-level plans and progress of these teams, managing projects from pre-clinical stages through to commercialization. The DDPM...
Global Study Manager - Oncology As a Global Study Manager at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives. What You Will Do: You will man...
Senior Local Trial Manager - Oncology (solid tumor) - Home Based (US) The Senior LTM role will be accountable/responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of...
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