Senior Oncology Clinical Research Associate - On-site Monitoring Pro
ICON Strategic Solutions
ICON plc, a world-leading healthcare intelligence and clinical research organization, is seeking a Senior Clinical Research Associate – Oncology to serve as the primary site liaison and monitor clinical sites. You will conduct all types of site visits, ensure ICH-GCP compliance, maintain CTMS/eTMF documentation, and support patient safety and data integrity across oncology programs. This on-site role requires a life sciences degree or RN, 3+ years’ monitoring experience, and up to 50% travel in #J-18808-Ljbffr ICON Strategic Solutions
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$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON is a global healthcare intelligence... ...will be doing: Implements and monitors clinical trials to ensure sponsor... ...of potential investigative sites, initiates clinical trials at investigative...SeniorWebsiteFull timeWork experience placementLocal areaRemote workWork visa- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology & hematology industry Industry Hospital... ...for investigative sites and sponsors, and... ...experience in medical research or clinical...SeniorWebsite
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...Oncology Sr. CRA 2 Our FSP team is currently seeking... ...2 with 5+ years of monitoring residing in the NYC Metro... ..., knowledge, and clinical judgement to provide a... ...situations based upon clinical research standards.... ...all aspects of study site monitoring including routine...SeniorWebsiteWork at officeLocal areaNight shift$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - New York ICON plc is a world-leading healthcare intelligence and... .... Responsibilities: Perform site management activities to support... ...sites Perform remote and on-site monitoring/co-monitoring visits (Site...SeniorWebsiteRemote jobWork experience placementInterim roleLocal areaFlexible hours- ...A leading organization in clinical research is seeking a Clinical Research Associate to ensure that clinical studies are conducted in compliance with... ...requirements. The role involves significant travel, monitoring clinical sites, and maintaining robust documentation while...SeniorWebsiteRemote work
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...CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1... ...Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full... ...OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key...WebsiteFull timePart timeImmediate startWorldwide- ...Kelly Science and Clinical FSP is currently seeking... ...a Regional Clinical Research Associate for a long-term engagement... ...sick/personal time. Senior Clinical Research... ...cardiovascular medical device monitoring experience- however,... ...identify issues at sites and implement...SeniorWebsiteFull time
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- ...commercialization lifecycle - from clinical trial support to real-world... ...experience.Brief Description:Monitors clinical trials and... ...protocol adherence, managing site activities, and overseeing data... ...Sites, Foundations, and local Research & Development Departments in...SeniorWebsiteContract workWork at officeLocal areaRemote work
- Celerion is seeking a full-time Lead, Clinical Research Associate to oversee monitoring and site management for clinical trials and related studies. You will lead a team of CRA staff, ensure timely delivery, and maintain GCP compliance while collaborating with sponsors...WebsiteFull time
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$110.52k - $138.15k
...Senior Clinical Research Associate- Northeast ICON plc is a world-leading healthcare intelligence and clinical... ...Do You will lead on clinical trial monitoring tasks requiring technical depth,... ...Responsibilities Include Monitoring clinical trial sites to ensure adherence to study...SeniorWebsiteWork experience placementFlexible hours- ...and support our Full Service Outsourcing team from major US hubs with 60-70% travel. The role focuses on monitoring, site management, and data integrity across clinical trials. Applicants should have a university degree or allied health certification and 6 months to 2...SeniorWebsiteRemote job
$92.32k - $126.94k
...clear economic value, better clinical outcomes and improved... ...the day to day operations associated with the execution of... ...clinical trials. He / she will monitor multiple clinical trial sites and studies. The primary... ...aspects of clinical research and regulatory regulations...SeniorWebsiteTemporary workWork experience placementInterim roleWorldwide
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