Clinical Research Associate I - Pediatric Trials & Data
Montefiore Hudson Valley Collaborative
Montefiore Hudson Valley Collaborative seeks a Research Associate to support the implementation and coordination of a NIH-funded research portfolio led by Dr. Marina Reznik. You will assist with clinical trials and community-based studies across clinical, school-based, and community settings, ensuring adherence to GCP and protocols while coordinating sponsor communications and regulatory documentation. The role includes data collection, management, and analysis, participant recruitment, and #J-18808-Ljbffr Montefiore Hudson Valley Collaborative
$58.66k - $81.68k
...Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities... ...Identifies and documents data errors or items requiring clarification... ...country’s best in several pediatric specialties. The Icahn School...DataTraineeshipLocal area$62.6k - $97.1k
...Informed by basic research done at our Sloan... ...translational and clinical research that is driving... ...at MSK: Join our Pediatrics - Transplant,... ...Clinical Research Associate ! This position offers... ...team encompassing data and patient... ...to ensure smooth trial execution. Perform...DataFull timeWork at office- Partner Company is seeking a Clinical Trial Monitor to oversee wound care studies with a focus on data integrity and regulatory compliance. You will conduct qualification and visitation activities across study sites, ensuring CRF accuracy and timely safety reporting. The...DataRemote job
- ...seeks a diligent professional to coordinate research portfolio activities, maintain real-time... ..., and serve as a central liaison among data management, patient coordination, and regulatory... ...solutions while ensuring smooth trial execution. On-site schedule five days a week...Data
- BeOne Medicines Ltd. seeks an experienced Clinical Research Associate (CRA) to monitor Oncology and Hematology trials across the United States. You will ensure protocol compliance, data integrity, and timely site visits, while collaborating with cross-functional teams to...Data
- ...alternative application process. CRO-Clinical Trials Assistant (remote) Full Time... ...in the review of clinical data at the case report form,... ..., correspondence, and associated documentation. Performs data... ...knowledge of applicable clinical research requirements, including GCP...DataRemote jobFull time
- ...fully integrated platform in terms of research and development, clinical development, manufacturing and... ...monitoring plans. Perform source data review (SDR), source data verification... ...Minimum 2 years of direct oncology trial monitoring experience (Phase I–III/IV...DataWorldwide
- ...The Clinical Research Associate (CRA) has local responsibility for the delivery of studies at allocated... ...to ensure proper delivery of clinical trials. This is a field-based position with... ...monitoring visits, including remote data review activities, in accordance with...DataHourly payTemporary workLocal areaRemote workFlexible hours
- The Mount Sinai Health System in New York, NY seeks a Clinical Research Associate I to monitor all aspects of the clinical trial life cycle, from site management through study closure, across Phases I-IV and post-marketing studies. Responsibilities include preparing essential...
- A medical device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical...Remote job
- ...to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. The CRA executes clinical monitoring activities at trial sites and ensures compliance with ICH/GCP and BeOne SOPs. Travel up to 60% to support oncology/hematology trials...
$74.5k - $197.5k
...study(ies) and reporting study data as required by the study... ...contracted scope of work and Good Clinical Practice. • Work with... ...available for filing in the Trial Master File (TMF) and verify... ...monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or...DataFull timePart timeLocal areaImmediate startWorldwide- ...of the City of New York's Division of Movement Disorders is seeking a Research Assistant to support clinical studies and patient interactions within a multidisciplinary team. The role involves data collection, regulatory submissions, data entry, and collaboration with...DataWeekend work
- IMPRESSION RECRUITMENT LIMITED is recruiting a Research & Trials Technician to join our established technical team in Bradford. This hands-on role combines practical lab work with data collection, analysis and technical reporting, supporting a range of projects and ensuring...Data
- Novo Nordisk is seeking a Clinical Trial Site Coordinator in New Jersey to oversee site engagement, trial start-up, patient recruitment, retention, and data management to ensure timely delivery of studies. The role requires strong communication with IRBs, vendors, and...DataRemote job
- NYU Grossman School of Medicine is seeking a Research Associate to support clinical trials and cohort studies in dialysis centers across New York City. This... ..., including early mornings and evenings, and involves data collection, patient recruitment, chart abstractions,...DataDaily paidFlexible hoursAfternoon shiftEarly shift
- Job Title: Clinical Research Associate II (CRA II) Job Location: United States - Remote Job Overview: The... ...sites throughout the clinical trial lifecycle. The CRA II serves as the primary... ...study teams to ensure subject safety, data quality, regulatory compliance, and successful...DataInterim roleRemote work
- ...house CRA in the United States to support clinical sites from approval through close-out,... ...field CRAs and Project Managers to ensure trial data integrity while maintaining regulatory... ...documentation, with 1-2 years in clinical research and permanent US work authorization. #J...DataRemote jobPermanent employment
- Role: Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country... ..., managing all phases of clinical trial conduct at assigned sites. Objectives:... ...in GCP, clinical trial processes, and data management; fluent in local language...DataRemote jobWork experience placementLocal area2 days per week3 days per week
- Role Role: Clinical Trial Site Coordinator at Novo Nordisk, responsible for site engagement, trial start-up, patient recruitment, retention, and data management to ensure successful trial delivery. Responsibilities Responsibilities include acting as primary site contact...DataRemote work
- ...quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,50... ...the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find... ...compliance, patient safety, and veracity of data. Review CRFs using paper or...DataInterim roleWork at officeWorldwide
- Position Summary The Clinical Research Associate (CRA) is responsible for monitoring clinical trial sites to ensure studies are conducted, recorded, and reported in accordance... .../CRO and investigative sites, safeguarding data integrity and patient safety throughout the...DataWork at officeLocal areaFlexible hoursAfternoon shift
- Overview As a clinical research associate (CRA), you are responsible for completing clinical research and... ...functioning and completion, evaluate clinical data, and create reports based on findings. Responsibilities Develop and write trial protocols (outlining purpose and...DataRelocationVisa sponsorship
- ...forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with... ...are performed according to the trial protocol and in compliance with SOPs,... ...of contact and ensuring high-quality data collection. Identify and resolve site...DataWork at officeRemote workFlexible hours2 days per week
- Clinical Research Associate - Oncology - OH/PA/VA At ICON Strategic Solutions, you will work in a sponsor... ...Do: You will contribute to clinical trial monitoring activities, taking responsibility... ...trials. Ensuring protocol compliance, data integrity, and patient safety...DataWorldwideFlexible hours
- ...quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,50... ...Department does at Worldwide Clinical Research Associates (CRAs) play a vital role in ensuring... ..., patient safety, and veracity of data. Review CRFs using paper or electronic...DataRemote jobInterim roleWork at officeWorldwide
$91.34k - $114.17k
Clinical Research Associate, Onc/Hem At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON... ...II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments...DataWorldwide- ...-based therapeutics. Primary Role The Clinical Research Associate (CRA) is responsible for the oversight... ...close out. The CRA assists the Clinical Trial Manager and/or Clinical Project... ...to ensure enrollment, timely review of data, identification of site issues, and prompt...DataInterim roleRemote work
$4,000 - $9,000 per month
...Clinical Research Associate DotLab is transforming the diagnosis and management of endometriosis, a... ...our team and support DotLab clinical trials. This role will initially focus on conducting... ...visits including monitoring of study data in accordance with the study...DataWork experience placementWork at officeRemote workWorldwideFlexible hours- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...that might affect subject safety and data integrity. Assess site processes per... ...and completeness, reconcile it with the Trial Master File (TMF), and ensure sites...DataInterim roleLocal areaImmediate startRemote workFlexible hours
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