Clinical Trial Associate
3 weeks ago
Clinical 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 us on our mission to shape the future of clinical developmentICON 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 developmentAs 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 requirementsResponsible 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 stakeholdersParticipate in the development of core trial documents and trial level plans, as requestedParticipate 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 dataParticipate in feasibility assessment and selection of countries and sites for trial conductParticipate in CRO and vendor set-up and management during clinical trial execution, as requested by clinical trial lead and/or clinical teamParticipate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverablesParticipate in CRO and vendor set-up and management during clinical trial execution, as requested by clinical trial lead and/or clinical teamEnsure quality and completeness of TMF for assigned clinical trialsParticipate in trial team meetings and manage associated documentation as requestedParticipate in data cleaning and data review activities as requestedParticipate in or lead set-up and implementation of effective investigator and site monitor trainingParticipate in the coordination and implementation of patient-focused strategies for assigned trials, as applicableResponsible for complying with regulations, GCP, SOPs and established standards during trial set-up, conduct and close-outYour Profile:BA/BS degree with at least two years clinical trial experienceMust 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 monitoringRequires project management skills and trial leadership abilityMust have excellent interpersonal, written and verbal communication skills, administrative skills and computer abilityFluent in EnglishModerate (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- 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...
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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 to...
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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
6 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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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...
