Clinical Research Coordinator I: Study Data & Consent
Mount Sinai Medical Center
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 source documents, shipping specimens as required, and preparing for monitoring visits. Qualifications include a Bachelor's or Master's in Science; no experience required with a preference for 1 year of research experience. #J-18808-Ljbffr Mount Sinai Medical Center
- 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...Data
- 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...Data
- Mount Sinai Health System is seeking a Clinical Research Coordinator I to support NIH All of Us study activities. Responsibilities include obtaining informed consent, collecting data, processing biospecimens, and assisting with IRB and grants documentation. Collaboration...Data
- 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...Data
- 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...Data
- 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.... ...grants documents and participate in study-related tasks across a major NIH initiative...Data
- 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...Data
- ...Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical research activities at a... ...site. 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
- 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...DataHourly payPart time
- The Mount Sinai Health System is seeking a Research Coordinator to support daily operations in a Psychiatry and Ob/Gyn lab in New York... .... You will also perform EHR abstraction, monitor data quality, track study spending, order supplies, and assist with REDCap and #J...Data
- ...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
- ...Health System in New York, NY seeks a Research Coordinator to support psychiatric and obstetric research... ...them, schedule visits, and conduct study visits including pregnancy and mental... ...The role also covers EHR abstraction, data QC, budget tracking, and assistance with...Data
- Mount Sinai Health System seeks a Clinical Research Coordinator to coordinate clinical assessments and assist... ...moderately complex research data. You will prepare grant applications and... ...completed. Responsibilities include screening study subjects, chart data compilation, and...DataWork at office
$17 - $38.48 per hour
...The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research... ...activities of clinical research studies, obtains informed consent; collects, maintains and... ...1. Collects and records study data. Inputs all information into database...DataHourly payPart timeTraineeshipWork at officeLocal area- DescriptionThe Clinical Research Coordinator is an entry human subjects researcher,... ...assisting in clinical research studies under the supervision of... ...individual obtains informed consent, collects, maintains and... ...and review of experimental data for publication and presentation...DataHourly payTraineeshipWork at officeLocal area
$26.77 - $40.05 per hour
...Informed by basic research done at our Sloan... ...translational and clinical research that is driving... ...Clinical Research Coordinator (CRC) to join the... ...management and data management on research/clinical studies.Role Overview:... ...study enrollment and consent processAssist the...DataFull timeMonday to FridayFlexible hoursShift workAfternoon shift$58.66k - $73.53k
...Job Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information... ...Collects and records study data. Inputs all information into database...DataTraineeshipWork at officeLocal area$66.3k - $70k
...Pediatrics is seeking a full-time Clinical Research Coordinator to join our team working on... ...of Health funded study to learn more about Crohn's... ...PI. Participate in the consent/assent process ensuring the... ...key personnel including the Data Coordinating Center at Connecticut...DataFull timeTemporary workLocal areaImmediate startFlexible hours$70.48k - $74.79k
...education, scientific research, and direct patient... ...join our team as a Clinical Research Coordinator.The Oncology Clinical... ...CRC performs study coordination tasks under... ...Coordinators (CRCs), Data Coordinator Unit (DCU... ...screening, through the consenting process, through the...DataWork at office- ...Clinical Research Coordinator (CRC) II A Clinical Research Coordinator (CRC) II position... ...will include activities such as data collection and management of patient... ...as required, obtain informed consent, collect, maintain and organize study information, and assist with...DataFull timeTraineeshipWork at officeLocal areaShift work
- ...Description The Parsons Research Center for... ...of Traumatic Stress Studies, joint projects of the... ...opening for a full-time clinical research coordinator to oversee day-to-day... ...: obtaining informed consent, screening participants... ...review of experimental data for publication and...DataHourly payFull timeTraineeshipLocal areaRemote work
- ...Job Description The Clinical Research Coordinator is an entry human subjects researcher... ...in clinical research studies under the supervision of the... ...obtains informed consent, collects, maintains and organizes... ...and review of experimental data for publication and presentation...DataHourly payTraineeshipWork at officeLocal area
- 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...Data
- The Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist in preparing grant applications and IRB filings. Responsibilities...Data
- 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...Data
- ...Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study information,... ...Grants and Contracts Office). You will input data into databases, maintain source...DataWork at office
- ...Morningside is seeking an entry-level Clinical Research Coordinator to conduct and assist in clinical studies under supervision. The role involves obtaining informed consent, collecting and organizing study... ...responsibilities such as data maintenance, participant screening...Data
$58.66k - $73.53k
Mount Sinai Medical Center is looking for a Clinical Research Coordinator to assist in daily activities of clinical research studies. Responsibilities include collecting data, obtaining informed consent, assisting in research activities, and preparing grant applications...Data- 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...Data
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