Clinical Research Coordinator I Data & Consent
mountsinai.com
Mount Sinai in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and collect and organize study information. Responsibilities include data collection and entry, consent processes, participant screenings, grant preparation, IRB submissions, and maintenance of source documents and regulatory files.
Qualifications include a Bachelor's or Master's degree in science or closely related field; no experience is required,
#J-18808-Ljbffr- ...The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data. You will assist in grant preparation, IRB submissions, and ensure compliance with hospital procedures...Data
- Mount Sinai Health System is seeking a Clinical Research Coordinator to support the daily activities of... ...clinical research studies, obtain informed consent, and manage study information. You... ...Responsibilities include collecting data, maintaining source documents, and...DataWork at office
- Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. You will assist in preparing grant documents, maintain source records, and help coordinate regulatory...Data
- ...Health System in New York, NY is seeking a Clinical Research Coordinator to help manage daily activities of clinical studies, obtain informed consent, and organize study information. You... ...-related documents, IRB submissions, data entry, subject recruitment, and specimen...Data
- The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical research activities at a... ...The role involves collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks under supervision...DataPart time
- Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant-related documents under supervision. This hourly role qualifies for overtime as needed...DataHourly payPart time
- DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for... ...not limited to: obtaining informed consent, screening participants for eligibility... ...analysis, and review of experimental data for publication and presentation....DataHourly payTraineeshipLocal area
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- ...Health System in New York City seeks a Clinical Research Coordinator to coordinate the clinical... ...interpretation of moderately complex research data. You will prepare grant applications... ...The role includes obtaining informed consent, mentoring coordinators, and ensuring...Data
- ...Mount Sinai Morningside in New York seeks a Clinical Research Coordinator to coordinate clinical assessments, analyze moderately complex data, and assist with protocol submissions.... ...Under supervision, you will obtain informed consent, monitor study subjects, and support...Data
- ...Mount Sinai Morningside in New York City seeks a Clinical Research Coordinator (CRC) I to join the Tisch Cancer Center. You will perform data collection, specimen collection, obtain informed consent, and help organize study information under supervision. The role supports...Data
- The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing... .... Collect and record study data and input all information into a database...DataTraineeshipWork at officeLocal area
- ...Mount Sinai is seeking an entry-level Clinical Research Coordinator to support dementia-focused studies... ...Americans. You will obtain informed consent, screen participants, and conduct bilingual... ...supervision. You will assist with data collection, documentation, and...Data
- ...associates, please click here. Overview Clinical Research Coordinator I will oversee multiple clinical... ...co-author input, and preparing study data for presentation and submission to... ...required training. Screens and consents patients and ensures the scheduling and...Data
$72.88k - $116.69k
...reconciles and interprets highly complex clinical research data; conducts clinical testing and... ...IRB/GCO documents are submitted. Coordinates protocols and human subject approvals... ...clinical trials. May obtain informed consent under general supervision of the Investigator...Data$66.3k - $68.3k
...posting. Position Summary The Clinical Research Coordinator (CRC) will support investigator-initiated... ...manager, a biostatistician, and a data manager to execute high-quality academic... ...eligibility and coordinate informed consent per IRB-approved protocols....DataTemporary workLocal area$66.2k - $98k
...Description Under minimal supervision, coordinates the clinical assessments of the study subjects;... ...moderately complex clinical research data. Prepares grant applications and documents... ...clinical trials. Obtains informed consent under supervision of the Principal Investigator...DataTraineeshipWork at officeLocal area$58.66k - $73.53k
...Clinical Research CoordinatorThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists... ...:Collects and records study data. Inputs all information into...DataTraineeshipWork at officeLocal area$58.66k - $73.53k
...Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information... ...Responsibilities Collects and records study data. Inputs all information into database...DataTraineeshipWork at officeLocal area$58.66k - $73.53k
...Sinai are seeking a highly motivated Clinical Research Coordinator I to join a growing, multidisciplinary... ...participants and obtain informed consent under the supervision of study investigators... ...procedures. Coordinate clinical data and biospecimen collection, including...DataTraineeshipLocal area- ...Job Title: Clinical Research Coordinator Department: CCC | Sponsored Research Position Summary The Clinical Research Coordinator serves as a... ...Oversees participant recruitment, enrollment, informed consent, data collection, and follow-up activities. Schedules and conducts...DataLocal areaRemote workShift work
- ...Science 37 accelerates clinical research by expanding patient access to trials... .... The Clinical Research Coordinator fulfills the requirements of... ...participates in the informed consent process, and enrolls... ...Responsible for accurate and timely data collection, documentation,...DataFull timeContract workTemporary workLocal area
- ...Clinical Research Coordinator (CRC) IIA Clinical Research Coordinator (CRC) II position is currently available... ...will include activities such as data collection and management of patient... ...entities as required, obtain informed consent, collect, maintain and organize study...DataTraineeshipWork at officeLocal areaShift work
- ...Clinical Research CoordinatorIntegrated in the Center for Regenerative Medicine... ...CRM), the Clinical Research Coordinator will work closely with... ...office setting and the OR, data management activities while... ...Oversees and conducts the informed consent process on studies as...DataWork at officeLocal areaFlexible hours
- ...the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Runs portions of... ...closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen...DataDaily paidFull timeTemporary workPart timeWork at officeRemote workFlexible hoursShift work
- ...Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for... ...staff. This individual obtains informed consent, collects, maintains and organizes... ...community education programs Maintain all data Qualifications ~...DataHourly payTraineeshipWork at officeLocal areaFlexible hours
- ...Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for... ...staff. This individual obtains informed consent, collects, maintains and organizes... ...analysis, and review of experimental data for publication and presentation....DataHourly payTraineeshipWork at officeLocal area
- ...Associate Clinical Research CoordinatorResearch -- AdministrationNew York... ...team as a Clinical Research Coordinator. The Oncology Clinical Research... ...Coordinators (CRCs), Data Coordinator Unit (DCU) staff... ...pre-screening, through the consenting process, through the screening...DataFull time
- ...within Mount Sinai's Icahn School of Medicine invites applications for a Clinical Research Coordinator I. Responsibilities include data collection, specimen handling, obtaining informed consent, and maintaining study records under supervision. The role supports clinical...Data
- Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and collect, organize, and maintain study... ..., and ensuring proper documentation and data integrity. Responsibilities include data...Data
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