Clinical Research Coordinator: Data, Consent & Grants
Mount Sinai
The Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and manage study data. This role involves assisting with grant-related documents and IRB/GCO submissions within a leading academic medical center. Qualified candidates typically hold a Bachelor's or Master's degree in science, with no experience required and one year of research experience preferred. #J-18808-Ljbffr Mount Sinai
- Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and maintain study data. You will assist with grant documents and IRB submissions, ensure proper source documentation, and help with...DataGrants
- Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB-related documents. Responsibilities include...DataGrants
- Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist in grant applications and IRB submissions. The role involves maintaining...DataGrants
- The Mount Sinai Health System is seeking a Clinical Research Coordinator to assist in daily study activities, obtain informed consent, and organize research data. You will help prepare grant-related documents and ensure compliance with IRB requirements. This role requires...DataGrants
- Mount Sinai Health System seeks a Clinical Research Coordinator I to assist in daily clinical research activities, obtain informed consent, and support data collection and specimen processing. You will help prepare IRB and grants documents and participate in study-related...DataGrants
- ...Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical... ...collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks... ...for sponsorship, and supporting grant applications and IRB submissions,...DataGrantsPart 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...DataGrantsHourly payPart time
$17 - $38.48 per hour
...The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical... ...studies, obtains informed consent; collects, maintains and... .... Assists in preparing grant applications and documents... ...Collects and records study data. Inputs all information into...DataGrantsHourly payPart timeTraineeshipWork at officeLocal area- DescriptionThe Clinical Research Coordinator is an entry human subjects researcher,... ...individual obtains informed consent, collects, maintains and organizes... ...and submission of grant applications and documents... ...and review of experimental data for publication and presentation...DataGrantsHourly payTraineeshipWork at officeLocal area
- Mount Sinai Health System is seeking a Clinical Research Coordinator I to support NIH All of Us study... ...Responsibilities include obtaining informed consent, collecting data, processing biospecimens, and assisting with IRB and grants documentation. Collaboration with...DataGrants
- Mount Sinai Morningside is seeking a Clinical Research Coordinator I to support daily activities of clinical studies, obtain informed consent, collect data, and assist with biospecimen handling. You will help prepare grant documents and ensure proper documentation in IRB...DataGrants
- Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist in preparing grant documents. Responsibilities include data entry, screening...DataGrants
- ...Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB/GCO submissions....DataGrants
- ...System in New York seeks a Clinical Research Coordinator to support daily activities... ...clinical studies, obtain informed consent, collect and organize study... ..., and assist in preparing grant documents (IRB, Grants and... ...Office). You will input data into databases, maintain...DataGrantsWork at office
- Mount Sinai Morningside is seeking a Clinical Research Coordinator to support human subjects research under the supervision... ...of senior staff. You will obtain informed consent, collect and organize study data, and assist in grant submissions and regulatory documents. The...DataGrants
- ...is seeking an entry-level Clinical Research Coordinator to conduct and assist in clinical... ...obtaining informed consent, collecting and organizing... ...information, and supporting grant applications and regulatory... ...includes responsibilities such as data maintenance, participant...DataGrants
- Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications, IRB submissions, and regulatory filings. The role...DataGrants
$58.66k - $73.53k
...Sinai Medical Center is looking for a Clinical Research Coordinator to assist in daily activities of clinical... .... Responsibilities include collecting data, obtaining informed consent, assisting in research activities, and preparing grant applications. Candidates should have a...DataGrants- Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, collect and organize study data, and assist in preparing grant documents (IRB, Grants and Contracts Office). Responsibilities...DataGrantsWork at office
$58.66k - $73.53k
...Job Description The Clinical Research Coordinator assists in the daily activities... ...studies, obtains informed consent; collects, maintains and organizes... .... Assists in preparing grant applications and documents... ...Collects and records study data. Inputs all information...DataGrantsTraineeshipWork at officeLocal area- ...Sinai Health System seeks an entry-level Clinical Research Coordinator to assist in conducting human subjects research... ...supervision. You will be involved in consent processes, data collection and organization, and support for grant-related documentation. You will help...DataGrants
- ...Description The Parsons Research Center for... ...opening for a full-time clinical research coordinator to oversee day-to-day... ...aspects of study design, grant preparation and/or... ...: obtaining informed consent, screening participants... ...of experimental data for publication and presentation...DataGrantsHourly payFull timeTraineeshipLocal areaRemote work
- ...Job Description The Clinical Research Coordinator is an entry human subjects researcher... ...obtains informed consent, collects, maintains and organizes... ...and submission of grant applications and documents... ...and review of experimental data for publication and presentation...DataGrantsHourly payTraineeshipWork at officeLocal area
- ...System is seeking an entry-level Clinical Research Coordinator to support clinical studies... ...supervision. You will obtain informed consent, collect and manage study data, and assist in regulatory... ...documents, and helping prepare grant materials. Strong organizational...DataGrants
- 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 applications. The role emphasizes accurate data handling, regulatory documentation,...DataGrantsPart time
$72.88k - $116.69k
...and interprets highly complex clinical research data; conducts clinical testing... ...negotiation. May prepare and ensure grant applications, IRB/GCO documents are submitted. Coordinates protocols and human subject... .... May obtain informed consent under general supervision of...DataGrants$16.5 - $38.48 per hour
Description The Clinical Research Coordinator, Part-time performs all the regular duties... ...studies, obtains informed consent, collects, maintains, and... ..., and assists in preparing grant applications and documents... ...Collects and records study data and inputs all information...DataGrantsHourly payPart timeTraineeshipWork at office- Mount Sinai Health System is seeking a part-time Clinical Research Coordinator to support daily study activities, consent participants, collect data, and assist with grant submissions. The role involves handling study documentation, data entry, and coordinating with sponsors...DataGrantsHourly payPart time
$70.48k - $88.24k
Position Summary Senior Clinical Research Coordinator (Senior CRC) at NYU Grossman School... .... Obtain informed consent and assent for adult and pediatric... ...accurate and timely data entry in sponsor EDC systems... ...protections. Experience with grant‑funded, industry‑sponsored,...DataGrantsWork at officeRemote work$66.3k - $75k
...Investigator(s) (PI) and the Clinical Research Supervisor (CRS), the Research Coordinator (RC) will be... ...Assistance in research grant preparation and administration... ...protocol development, consent form preparation,... ...progress reports Research data collection, entry and...DataGrantsFull timeTemporary workPart timeLocal areaWeekend workAfternoon shift
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