Clinical Trials Research Associate - Data Capture & Study Coordination
Montefiore Orthopedics
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 Montefiore Orthopedics
- ...Clinical Research Associate For Clinical Study Coordinators located in Berlin: The Clinical Research Associate role at Medpace... ...against case report form data, including informing the site staff... ...through our integrated Clinical Trial Management System to identify site...DataContract workWork at officeRemote workWork from homeFlexible hours
- ...exploring ways to address data gaps, our mission... ...and integrity of clinical data. Your work will... ...this role, you will: Coordinate and support clinical trial activities,... ...Project Managers and Study Managers, assisting... ...with electronic data capture systems Experience using...DataWork at officeLocal areaWorldwide
- Position Summary The Clinical Research Associate (CRA) is... ...monitoring clinical trial sites to ensure studies are conducted, recorded... ...sites, safeguarding data integrity and... ...investigators, site coordinators, and study staff Track... ...Electronic Data Capture (EDC) systems and...DataWork at officeLocal areaFlexible hoursAfternoon shift
- ...and strengthen our Clinical Operations team.... ...knowledge of clinical research processes and... ...monitoring clinical trials and Ensuring that... ...Ensuring data quality and integrity... ...patients involved in a study are protected Performing and coordinating all aspects of the...DataPart timeFreelanceLocal areaRemote work
$58.66k - $81.68k
...Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including... ...Estimates, orders and coordinates shipments of clinical study... ...Identifies and documents data errors or items requiring...DataTraineeshipLocal area$85k - $95k
...translational research. We're bringing... ...labs to mobile clinics. By helping providers... ...Research Associate (CRA) is responsible... ...clinical trials at external clinical... ...clinical study protocol execution... ...ensuring timely data collection and... ...including site coordination, investigational...DataHourly payRemote workWork from homeWorldwideFlexible hoursNight shift- ...therapeutics. Primary Role The Clinical Research Associate (CRA) is responsible... ...assists the Clinical Trial Manager and/or... ..., timely review of data, identification of site... ...and other relevant study information Conduct Site... ...Assist with the coordination and conduct of investigator...DataInterim roleRemote work
- ...oncology for breast cancer clinical studies is hiring a Remote Clinical Research Associate to work in the United... ...be responsible for coordinating clinical study... ...clinical documentation and data, and ensuring compliance... ...inconsistent data. Maintain the Trial Master File,...DataWork at officeRemote work
- ...the way we integrate clinical trial execution with deep scientific... ...and advanced data sciences. We have a... ...recruiting Clinical Research Associate II to join our team in... ...You identify potential study risks and propose... ...standards. You will coordinate all necessary activities...DataRemote workNight shiftDay shift
- ...recognized laboratory services, clinical trials, and reimbursement... ...technology platforms for real-time data and study transparency. Hiring... ...Summary: The Clinical Research Associate II (CRA II) participates... ...start-up department to coordinate activities with assigned sites...DataWork experience placementInterim roleWork at officeRemote work
$75k - $95k
...translational research. We’re bringing... ...labs to mobile clinics. By helping providers... ...Research Associate II is responsible... ...clinical trials at external clinical... ...Lead clinical study execution across... ...compliance, timely data collection,... ...Electronic Data Capture (EDC) systems,...DataHourly payContract workWork experience placementRemote workWork from homeWorldwideNight shift$47.03k - $66.3k
...education, scientific research, and direct... ...team as a Research Associate. This role involves clinical research data collection,... ...variable hours based on study needs,... ...as determined in coordination with the research... ...enrolled in clinical trials and cohort studies...DataDaily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift- ...POSITION TITLE: Clinical Research Associate II DEPARTMENT: Monitoring... ...integrated clinical data solutions, and global... ...Ora’s compliance of study conduct by monitoring... ...through all phases of the trial. Performs, with... ...related procedures. Coordinate & manage various tasks...DataDaily paidFull timeInterim roleLocal areaRemote workFlexible hours
- Montefiore New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a primary contact for patients and study teams. The role involves coordinating with multiple departments to... ...trial workflows, manage data entry and patient consent, and...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
- ...School of Medicine is seeking a per diem Research Associate to support clinical research data collection and interactions with study participants across dialysis centers in New... ...entry and cleaning, SOP maintenance, and coordination with #J-18808-Ljbffr NYU Grossman School...DataDaily paidFull timeFlexible hoursDay shiftAfternoon shiftEarly shift
$125k - $140k
...skills, knowledge, and clinical judgement to... ...participants in clinical trials and respond to... ...upon clinical research standards. Responsibilities... ...all aspects of study site monitoring... ...integrity of the data submitted on Case... ...co-monitoring Coordinate designated...DataWork at officeLocal areaNight shift- ...Pfizer seeks a Clinical Research Associate to manage and monitor assigned... ...across clinical trials. The role ensures patient... ..., and quality study execution through site... ...and cross-functional coordination from initiation through... ...protocol-related issues, data queries, and adverse...DataLocal areaRemote work
- ...dedicated and experienced Clinical Research Associate (CRA) to manage and... ...Phase III clinical trials across various... ...compliance of clinical trial data. Your expertise will... ...to investigators and study site staff on... ...and electronic data capture (EDC) systems. Excellent...DataDaily paid
$103k - $130k
...Sr. Clinical Research Associate Bring more to life. Are you ready... ...device clinical trials at external clinical... ...Oversee clinical study protocol execution at... ...out, ensuring timely data collection and compliance... ...monitoring, including site coordination, investigational...DataContract workRemote workWork from homeWorldwideFlexible hoursNight shift- 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
- ...excellence. We are Worldwide Clinical Trials, and we are a global... ...Worldwide Clinical Research Associates (CRAs) play a vital... ...site management, and study close-out visits.... ...safety, and veracity of data. Review CRFs using... ...or electronic data capture systems and assist sites...DataRemote jobInterim roleWork at officeWorldwide
- 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
- ...excellence. We are Worldwide Clinical Trials, and we are a global... ...as a Senior Clinical Research Associate at Worldwide Bring... ...expertise to studies where quality, patient... ...sites deliver reliable data while maintaining protocol... ...on global studies, coordinate and mentor CRAs,...DataRemote jobInterim roleWork at officeLocal areaWork from homeWorldwide
- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health® is... ...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...DataInterim roleLocal areaImmediate startRemote work
$24 - $29 per hour
...Shaping the Future of Clinical Research Adams Clinical... ...leading clinical trial site network... ...deliver uncompromising data quality, safety,... ...and outpatient studies. We are... ...confirm appointments, coordinate transportation,... ...Ensure accurate capture and upload of paper...DataHourly payWork at officeFlexible hours$82.7k - $137.9k
...The Senior Clinical Research Associate I is responsible for the site... ...of assigned clinical trials investigator sites to... ...patient safety and quality study execution in... ...of issues Resolve data queries within required... ...site selection, PTA, coordination of site activation checklist...DataPermanent employmentFull timeH1bLocal areaRemote workVisa sponsorshipWork visaRelocation packageWeekend work- ...invites applications for a Research Coordinator to support basic to moderate coordination of research studies at the Medical Center. The role... ..., grant submissions, data collection, and liaison with... ...guidelines while supporting ongoing clinical research activities. #J-188...Data
- The Clinical Research Coordinator at Mount Sinai Health System in New York City supports dermatology studies under the supervision of PI or senior staff, handling consent, data collection, and documentation. Responsibilities include coordinating participant screening,...Data
$75k - $80k
...looking for a seasoned Clinical Research Coordinator who is interested in... ...sites to work as a Study Coordinator. Weekend... ...coordinates the daily clinical trial activities and plays... ...accurately Collects data as required by the... ...the electronic data capture (EDC) system in the...DataDaily paidContract workRemote workWeekend work
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