Clinical Research Assistant: Data, IRB & Study Coordination
Weill Cornell Medicine - Qatar
Weill Cornell Medicine - Qatar is seeking a detail-oriented research assistant to support clinical studies. You will assist researchers with data collection, literature reviews, and protocol development, coordinating participant recruitment and data entry. The role requires familiarity with medical terminology, SPSS or REDCap, and an ability to handle multiple tasks in a fast-paced research environment. Bachelor's degree is preferred, with about one year of related experience. #J-18808-Ljbffr Weill Cornell Medicine - Qatar
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- The Research Foundation for Mental Hygiene... ...full-time Research Assistant to support an NIH-funded study focused on clinical trials. The... ...scheduling subjects, data entry, and assisting... ...include coordinating patient appointments... ...databases, helping with IRB #J-18808-Ljbffr...DataFull time
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- ...member of the research team in compliance... ...all research study related activities... ...assurance of data for the... ...activities and patient coordination; ensuring... ...Responsibilities include:Assist in the... ...development and build of Clinical Research... ...for research (IRB applications, conflict...DataLocal area
- ...Health System is seeking a Clinical Research Assistant I to support daily... ...activities of clinical research studies, including data collection and... ...preparing grant applications and IRB/GCO documents and provide... ...support to Clinical Research Coordinators in the assigned area....Data
$16.5 - $27.65 per hour
Description The Clinical Research Assistant II performs a wide variety... ...to clinical research study on behalf of the Tisch... ..., including data maintenance, and related... ...such as preparing and coordinating meetings with various... ...grant applications, IRB/GCO for submission and...DataHourly payTraineeship- ...New York, NY is seeking a Clinical Research Coordinator. This entry-level researcher assists in conducting clinical studies under supervision, obtains... .... Responsibilities include data collection, participant screening... ...role offers exposure to IRB processes and data...Data
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- ...System in New York is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent from... ...study information. You will assist in preparing grant applications and regulatory documents (IRB, Grants and Contracts Office)....DataWork at office
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- ...New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a... ...contact for patients and study teams. The role involves coordinating with multiple... ...study protocols under IRB and FDA regulations.... ...trial workflows, manage data entry and patient...Data
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- Description The Clinical Research Assistant I assists in the daily activities... ...of clinical research studies, including collection... ...to Clinical Research Coordinators and others in... ...Collects and records study data. Inputs all... ...grant applications, IRB/GCO for submission and...DataHourly payTraineeshipWork at officeLocal area
$24 - $29 per hour
...Shaping the Future of Clinical Research Adams Clinical is... ...deliver uncompromising data quality, safety, and... ...and outpatient studies. We are seeking... ...the Clinical Research Assistant role at our Bronx location... ...confirm appointments, coordinate transportation, and...DataHourly payWork at officeFlexible hours- ...Kettering Cancer Center in New York is seeking a Clinical Research Associate to support portfolio activities,... ...teams. You will help ensure study progress, communicate findings to partners, and assist with data management, regulatory oversight, and trial execution...Data
- ...Job Description The Clinical Research Assistant I assists in the daily activities of clinical research studies, including collection and organization... ...to Clinical Research Coordinators and others in assigned... ...enrollment, study coordination, data management, and research...DataPart timeTraineeshipWork at officeLocal area
$103k - $130k
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...the trial. Performs clinical study site management/monitoring... ...related procedures. Coordinates & manages various... ...various tools to ensure: Data generated at site are... ...externally with vendors and IRB/IECs and Regulatory... ...strong clinical research capabilities. Travel...DataRemote jobFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week- ...Morningside is seeking a Research Program Coordinator to support the implementation... ...-to-day coordination of a clinical study under the supervision of... ...recruit participants, collect data, manage the study database... ...research activities, assisting with enrollment and screening...Data
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- ...Biosciences is seeking a Senior Clinical Research Associate to manage and... ...setup. The Sr. CRA will support study planning, site startup, patient recruitment, data quality, and regulatory compliance... ..., develop study documents, coordinate data reports, review CRFs, and...DataRemote work
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...Clinical Research AssociateDotLab is transforming the diagnosis and management... ...including monitoring of study data in accordance with the study... ...applicable regulatory standards, IRB policies, and DotLab... ...are current and maintained; assist in audit readiness and preparation...DataWork at officeRemote workWorldwideFlexible hours- ...Job Description - Clinical Research Assistant (2602668) Clinical Research Assistant Required Qualifications... ...and using special methods for data collation and interpretation. Fluent in... ...the Aging in Kerala Americans Research study. The ideal applicant will have the ability...DataFull timeCasual workWork at officeShift workAfternoon shift
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$58.66k - $81.68k
...Description Job Description The Clinical Research Associate I monitors... ...trial(s) Clinical study life-cycle... ...Estimates, orders and coordinates shipments of clinical... ...assigned investigator sites. Assists the CTM with tracking... ...Identifies and documents data errors or items requiring...DataTraineeshipLocal area$105k - $117k
...skills, knowledge, and clinical judgement to... ...based upon clinical research standards.... ...for all aspects of study site monitoring including... ...integrity of the data submitted on Case... ...assigned by management Assist with training of... ...g., co-monitoring Coordinate designated...DataWork at officeLocal areaRemote workFlexible hours- ...Summary Job Description The Senior Clinical Research Associate (Sr. CRA) is an... ...across multiple clinical studies. This role serves as a key resource... ...(GCP, FDA, ISO), IRB/EC requirements, and company... ...and maintain accurate study data in clinical systems, including...DataHourly payContract workRemote workShift work
$82.7k - $137.9k
...The Senior Clinical Research Associate I is responsible for... ...safety and quality study execution in accordance... ...of issues Resolve data queries within... ...site selection, PTA, coordination of site activation checklist... .... Relocation assistance may be available based...DataPermanent employmentFull timeH1bLocal areaRemote workVisa sponsorshipWork visaRelocation packageWeekend work- ...senior Project Manager Federal Health IT & Study Data Experience: 8 12 Years... ...Domain:** Federal Health IT / FDA / NIH / Clinical & Nonclinical Study Data Only... ...planning, demonstrations, retrospectives, and coordination across development, testing, security,...DataFull timeFor contractorsFor subcontractorRemote work
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