Part-Time Clinical Research Coordinator: Data & Consent
Internal Medicine
The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical research activities at a New York site. The role involves collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks under supervision. Responsibilities include data entry, participant screening, credentialing for sponsorship, and supporting grant applications and IRB submissions, with an emphasis on ensuring accurate documentation and #J-18808-Ljbffr Mount Sinai Health System
- 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...Part timeDataHourly pay
- 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
$16.5 - $38.48 per hour
Description The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator... ...research studies, obtains informed consent, collects, maintains, and organizes... ...Collects and records study data and inputs all information into the...Part timeDataHourly payTraineeshipWork at office- ...A part-time Clinical Research Coordinator (CRC) I position is currently available within the Tisch Cancer Center. Duties... ...include activities such as, but no limited to, data collection, specimen collection, obtaining informed consent, and maintaining and organizing study...Part timeDataTraineeshipLocal area
$17 - $38.48 per hour
...The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator,... ...research studies, obtains informed consent; collects, maintains and organizes study... ...). Collects and records study data. Inputs all information into database...Part timeDataHourly payTraineeshipWork at officeLocal area- DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects... ...: obtaining informed consent, screening... ...review of experimental data for publication and presentation... ...join us, you become part of Mount Sinai’s... ...challenges of our time — discovering and applying...DataHourly payTraineeshipLocal area
- DescriptionThe Parsons Research Center for... ...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... ...join us, you become part of Mount Sinai’s unparalleled...DataHourly payFull timeTraineeshipLocal areaRemote work
- NYU Langone Health is seeking a Clinical Research Coordinator in New York with oncology trial experience... ...patient safety, protocol adherence and data integrity under PI supervision and... ...include recruitment, screening, informed consent support, trial logistics,...Data
$58.66k - $73.53k
...Description The Clinical Research Coordinator assists in the daily activities... ..., obtains informed consent; collects, maintains... ...and record study data and input all information... ...ability to manage time appropriately, able to... ...join us, you become part of Mount Sinai’s unparalleled...DataTraineeshipWork at officeLocal area- ...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
- ...Langone Health is seeking an Oncology Clinical Research Coordinator to actively coordinate oncology... ...leadership, CRNs, and DCU staff to support data quality and regulatory adherence.... ...recruitment, pre-screening, informed consent discussions, tracking trial forms, and...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
- ...Morningside in New York, NY is seeking an entry-level Clinical Research Coordinator to support human subjects research under the... .... The role involves obtaining informed consent, collecting and organizing study data, and assisting with grant applications and regulatory...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
- Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and maintain study data. You will assist in preparing grant applications and IRB/GCO submissions, and ensure proper documentation...Data
- ...Sinai's Institute for Critical Care Medicine (ICCM) in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and organize study data. You will assist in grant preparation and IRB filings, and help ensure...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
- The Clinical Research Coordinator at Mount Sinai Morningside is an entry-level human subjects researcher responsible for conducting... ...staff. This role involves obtaining informed consent, collecting and organizing study data, and supporting regulatory submissions. You will...Data
- The Mount Sinai Health System is seeking a Clinical Research Coordinator to support investigators in conducting human subjects research. You will obtain informed consent, collect data, and help prepare study materials under supervision in a fast-paced academic setting....Data
- About Us At Rovia Clinical Research, we're on a... ...path, you'll be part of a team that truly... ...Clinical Research Coordinator (CRC) is responsible... ..., enrollment, data quality, and overall... ...Ensures informed consent is properly... ...appropriate. Completes timely and accurate...DataWork at officeLocal area
$70.48k - $74.79k
...to join our team as a Clinical Research Coordinator. The Oncology... ...Coordinators (CRCs), Data Coordinator Unit (DCU... ...screening, through the consenting process, through the... ...policies and ensuring a timely, accurate and complete... ...investigator, may take part in AE and Con Med documentation...DataWork at office$66.2k - $90k
Description A Clinical Research Coordinator (CRC) II position is currently available... ...include activities such as data collection and management of... ...clinical information, timely collection of protocol related... ...required, obtain informed consent, collect, maintain and organize...DataTraineeshipWork at officeLocal area- ...diagnostic, treatment, and research services. The Clinical Research Coordinator (CRC) supports the... ...recruitment, informed consent, scheduling, data management, and... ...completion, and ensure timely data entry and query resolution... ...independently and as part of a team. Strong...DataWork at office
$64.35k - $70k
Join to apply for the Clinical Research Coordinator - PACC role at Columbia University... ...compensation at the time of posting. Position Summary... ...limited to recruiting and consenting patients, conducting study... ...accurate source documentation and data entry. Collect, record, and...DataFull timeTemporary workWork at officeLocal area$70.48k - $88.24k
Position Summary Senior Clinical Research Coordinator (Senior CRC) at NYU Grossman School of Medicine... ...participants efficiently. Obtain informed consent and assent for adult and pediatric... ...signature. Perform accurate and timely data entry in sponsor EDC systems and...DataWork at officeRemote work- ...Job Description The Clinical Research Coordinator assists in the daily... ...studies, obtains informed consent; collects, maintains... ...and records study data. Inputs all information... ...join us, you become part of Mount Sinai’s... ...care challenges of our time — discovering and applying...DataWork at officeLocal area
- Position Summary Travel Clinical Research Coordinator plays a key role in supporting... ...close out Recruit, screen, consent, and enroll participants according... ...document accurate study data including source... ...adverse event reports Ensure timely and accurate electronic data...DataNight shiftAfternoon shift
$66.3k - $68k
...of possible compensation at the time of posting. Position Summary Clinical Research Coordinators (CRCs) are key members of... ...responsibilities include study coordination, data collection, regulatory... ...Focus Support recruitment and consenting activities for pharmaceutical company...DataTemporary workWork at officeLocal area$64.35k - $65k
...is recruiting for the position of a Clinical Research Coordinator (CRC). The employee will work within... ...assure compliance with study protocols, data documentation, reporting requirements... ..., upcoming protocol amendments, consent changes, and applicable protocol training...DataTemporary workWork at officeLocal areaFlexible hours$70.48k - $88.24k
...people. An integral part of NYU Langone Health... ..., scientific research, and direct patient... ...our team as a Senior Clinical Research Coordinator. The Senior Clinical... ...efficiently. Obtain informed consent and assent for adult... ...accurate and timely data entry in sponsor EDC...DataWork at officeRemote work
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