Clinical Trial Associate
3 weeks ago
Clinical Trial Associate- Remote Candidates must have experience managing sites in pharma/CRO setting Oncology experience required Experience with US sites preferred 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 us on our mission to shape the future of clinical development 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 us on our mission to shape the future of clinical development As a Clinical Trial Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing: Support the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements Responsible for maintaining accurate and up-to-date trial information within relevant tracking systems and provide regular updates as requested to trial team and other defined stakeholders Participate in the development of core trial documents and trial level plans, as requested Participate in or lead trial related systems set-up including implementation and maintenance of appropriate systems, standards and processes to ensure quality across investigative sites, vendors and data Participate in feasibility assessment and selection of countries and sites for trial conduct Participate in CRO and vendor set-up and management during clinical trial execution, as requested by clinical trial lead and/or clinical team Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables Participate in CRO and vendor set-up and management during clinical trial execution, as requested by clinical trial lead and/or clinical team Ensure quality and completeness of TMF for assigned clinical trials Participate in trial team meetings and manage associated documentation as requested Participate in data cleaning and data review activities as requested Participate in or lead set-up and implementation of effective investigator and site monitor training Participate in the coordination and implementation of patient-focused strategies for assigned trials, as applicable Responsible for complying with regulations, GCP, SOPs and established standards during trial set-up, conduct and close-out Your Profile: BA/BS degree with at least two years clinical trial experience Must have strong knowledge of ICH/GCP guidelines and regulatory requirements. Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring Requires project management skills and trial leadership ability Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability Fluent in English Moderate (10%) travel required
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Clinical Trial Associate
2 weeks ago
, , Canada ICON Strategic Solutions Full timeJoin to apply for the Clinical Trial Associate role at ICON Strategic Solutions . 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 us on our mission to shape the future of clinical development. We are...
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Clinical Trial Associate
2 weeks ago
, , Canada ICON Strategic Solutions Full timeClinical Trial Associate 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 us on our mission to shape the future of clinical development. We are currently seeking a Senior Site Management Associate to join our...
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Markham, Ontario, LRB, Canada Everest Clinical Research Full time $80,000 - $120,000 per yearEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...
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Clinical Trial Associate
3 weeks ago
Canada ICON Strategic Solutions Full timeClinical Trial Associate- RemoteCandidates must have experience managing sites in pharma/CRO settingOncology experience requiredExperience with US sites preferredICON 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...
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Clinical Trial Associate
3 weeks ago
Canada ICON Strategic Solutions Full timeClinical Trial Associate- Remote Candidates must have experience managing sites in pharma/CRO setting Oncology experience required Experience with US sites preferred 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...
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Clinical Trial Assistant
2 weeks ago
Canada NeuroRx Research Full time**The role**:The Clinical Trial Assistant provides administrative support to all Project Managers in their daily duties, including liaising with clinical sites and MRI facilities. These duties include but are no limited to the following: - Submit requests for shipment of MRI supplies and trial-specific sFTP account creation - Issuing trial-specific...
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Clinical Safety Data Associate
5 days ago
Markham, Ontario, LRB, Canada Everest Clinical Research Full time $60,000 - $80,000 per yearEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...
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Senior Clinical Trial IWRS Monitor
1 day ago
Markham, Ontario, LRB, Canada Everest Clinical Research Full time $70,000 - $90,000 per yearEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...
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Clinical Research Safety Associate
5 days ago
Markham, Ontario, LRB, Canada Everest Clinical Research Full time $60,000 - $80,000 per yearEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...
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Clinical Trial IWRS Monitor I
1 day ago
Markham, Ontario, LRB, Canada Everest Clinical Research Full time $45,000 - $65,000 per yearEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...
