Clinical Trials Research Associate - Data Capture & Study Coordination
ViziRecruiter,LLC.
ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed consent, and ensuring compliance with Good Clinical Practice. The ideal candidate should have a Bachelor's degree, with a Master's degree preferred, along with relevant certifications. Responsibilities include data collection, subject screening, and coordination of study activities. #J-18808-Ljbffr ViziRecruiter,LLC.
- A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...Data
- ...Medical Center in New York, NY is seeking a Clinical Research Assistant I to support daily clinical... .... The role involves assisting with study operations, handling participants, and... ...applications. The ideal candidate will have an Associates Degree in a related field and...Data
$38 - $40 per hour
...Baim Institute for Clinical Research Director, Human... ...Clinical Research Associate/Field Monitor... ...Interim Monitoring and Study Close-out Visits,... ...manner, in coordination with SM Lead and/... ...CRA Comply with Trial Master File (TMF)... ...Knowledgeable of Electronic Data Capture System (e.g...DataPart timeFor contractorsInterim roleRemote workWork from home10 hours per week$58.66k - $81.68k
...Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities... ...# Estimates, orders and coordinates shipments of clinical study... ...Identifies and documents data errors or items requiring...DataTraineeshipLocal area$103k - $130k
...translational research. We're bringing... ...labs to mobile clinics. By helping providers... ...Research Associate (Sr. CRA) is responsible... ...clinical trials at external... ...Oversee clinical study protocol execution... ...?timely?data collection and... ...including site coordination, investigational...DataHourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift$120k - $135k
...edge science and robust clinical pipeline form the... ...seeking a Senior Clinical Research Associate (CRA) to support our... ...overseeing clinical trial site management and... ...support high-quality study execution, patient recruitment... ...strategies, data capture, and site engagement...DataTemporary workWork at officeImmediate startVisa sponsorship- NYU Langone Hospitals in New York, NY is seeking a Research Associate (Per Diem) to join their Center for Surgical and... .... The primary responsibilities include supporting clinical research, participant recruitment, data collection, and documentation maintenance. This position...DataDaily paid
- ...in New York City is hiring a Clinical Research Assistant I to support daily... ...of clinical research studies. Responsibilities include collecting... ...and recording study data, assisting in grant applications... .... Candidates should have an Associate's Degree in Science or related...DataHourly pay
- ...responsible for performing study site management... ...the sponsor and clinical site Responsible... ...integrity of the data submitted on Case... ...and other trial records are accurate... ...interest in clinical research Strong knowledge... ...planning, organizing, coordinating, problem solving...Data
- Overview As a clinical research associate (CRA), you are responsible for... ..., evaluate clinical data, and create reports... ...Responsibilities Develop and write trial protocols (outlining... ...report forms (CRFs) Coordinate with the ethics... ...reports Archive study documentation and correspondence...DataRelocationVisa sponsorship
$60k - $80k
...Behavioral Medicine is seeking a Clinical Research Associate I. In this role the Clinical... ...Research Associate I will manage and coordinate a large-scale research study on temporomandibular disorders... ...examinations to obtain clinical data and to collect oral and biological...Data$103k - $130k
The Sr. Clinical Research Associate (Sr. CRA) is responsible for the setup... ...device clinical trials at external clinical... ...Responsibilities Oversee clinical study protocol execution at... ...out, ensuring timely data collection and... ..., including site coordination, investigational...DataContract workRemote workNight shift- Clinical Research Associate I/II Benefits include: Medical, Dental, and... ...’s ongoing clinical trials, in line with PMT’s corporate... ...the direction of study management. This... ...study success. PMT is a data‑driven company,... ...RESPONSIBILITIES Manage and coordinate in‑house clinical...DataLocal areaRemote workWorldwide
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated... ...affect subject safety and data integrity. Assess site... ...effective conduct of clinical study data review and capture, and verify site... ...completeness, reconcile it with the Trial Master File (TMF), and...DataInterim roleLocal areaImmediate startRemote workFlexible hours
$125k - $145k
Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas... ...with personnel from study Sponsors, investigational... ...of clinical trials in compliance with ICH... ...Meetings, CRA and Study Coordinator training sessions, and... ...and ensure continuous data flow (i.e., on‑time...DataContract workTemporary workInterim roleLocal areaRemote work- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a... ...patient's safety and clinical data integrity at an... ...conduct of the clinical study data review and capture. Verifies site compliance... ...contents of the ISF with the Trial Master File (TMF). Ensures...DataContract workInterim roleLocal areaImmediate startRemote workFlexible hours
$66.8k - $125k
...Description Join Us as a Clinical Research Associate (Level II) - Make an... ...2,700 clinical trials across 100+ countries... ...you will perform and coordinate all aspects of the clinical... ..., well-being, and data reliability. You will... ...as required. Ensures study systems are updated...DataTemporary workWork at officeRemote workHome officeFlexible hoursNight shift- Clinical Research Associate We're a global, midsize CRO that pushes boundaries... ...Worldwide Clinical Trials, and we are a global... ...site management, and study close-out visits.... ..., and veracity of data. Review CRFs using paper... ...or electronic data capture systems and assist sites...DataInterim roleWork at officeWorldwide
- Clinical Research Associate I/ Clinical Research Associate II Precision... ...of one to two studies setting you up to be... ...standards. You will coordinate all necessary activities... ...combining novel clinical trial designs, industry-leading... ...biomarker and data analytics solutions,...DataWork from homeNight shift
- Regional Clinical Research Associate II BIOTRONIK is one of the leading... ...II to our Clinical Studies team. Conduct on-... ...related areas by ensuring data integrity, subject... ...and Research Coordinators during monitoring visits... ...medical device IDE trials is preferred. Strong...DataWork at officeRemote workHome office
- ...will also monitor data quality and patient... ...aspects of the clinical monitoring process... ...Functions: Perform and coordinate assigned aspects... ...sites, and study vendors Provide protocol... ...global oncology trials preferred. Other Experience... ...of ICH and associated regulatory...DataLocal area
- Mount Sinai Morningside is looking for a Research Program Coordinator I to lead and assist in study protocols and data analysis. This role is essential for managing human subjects and laboratory research tasks, contributing to health interventions and their outcomes. The...Data
$66.2k - $90k
Mount Sinai Medical Center is seeking a Clinical Research Coordinator for NIH-funded studies at the Icahn School of Medicine. This role involves monitoring clinical trials and managing data analysis while engaging in clinical practice related to nutrition and exercise physiology...Data- Mount Sinai Medical Center in New York is looking for a Clinical Research Coordinator to support clinical research studies under supervision. This position involves obtaining informed consent, collecting data, and ensuring compliance with regulations. The ideal candidate...DataHourly pay
$58.66k - $73.53k
Mount Sinai Medical Center is hiring a Clinical Research Coordinator to assist with daily activities of clinical research studies. Responsibilities include collecting data, obtaining informed consent, and preparing grant applications. No experience is required, but one...Data- Lead Clinical Research Associate Work Flexibility: Remote Why Join Stryker... ...of clinical studies, working closely with... ...associated with the study. Coordinate clinical activities with... ...the proper conduct of trials. Monitor the quality of site data, identify discrepancies...DataLocal areaRemote work
$35 per hour
The University of Georgia is seeking a Research Associate to coordinate a long-term study on white-tailed deer movements in northeastern... ...in field research and large animal capture operations. The role involves field research, data management, and communication with state...DataHourly pay- ...Medical Center in New York seeks a Clinical Research Coordinator to manage and assist in clinical trials. The role involves conducting... ...research and organizing study information under supervision.... ...position is crucial for ensuring data accuracy and patient consent. The...DataHourly pay
$58.66k - $81.68k
Mount Sinai Medical Center is looking for a Research Program Coordinator I to develop and participate in study protocols, analyze data, and oversee human subjects in research. The ideal candidate will have a Master’s degree in Natural Sciences or a Bachelor’s with significant...Data$58.66k - $73.53k
...Sinai Medical Center in New York is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research studies. You will be involved in obtaining informed consent, collecting and maintaining study data, and assisting in grant applications. This...Data
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