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 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
- 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...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
$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- SiteBridge Research Inc: Founded in 2021, SiteBridge... ...sponsored clinical research on time and on budget,... ...unmet needs to take part in clinical... ...Clinical Research Coordinator (Long Island, NY)... ...obtaining informed consent, and conducting protocol... ...and interpret data, taking note of...Part timeDataLocal area
$66.3k - $75k
...compensation at the time of posting.... ...Investigator(s) (PI) and the Clinical Research Supervisor (CRS), the Research Coordinator (RC) will be... ...protocol development, consent form preparation,... ...reports Research data collection, entry... ...full-time and part-time students. Equal...Part timeDataFull timeTemporary workLocal areaWeekend workAfternoon shift- 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. Inputs all information into database...Part timeDataHourly payTraineeshipWork at officeLocal area
- 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,...Part timeData
- 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...Part timeDataHourly pay
- To support multiple clinical and health services research projects, the part-time per diem Clinical Research Coordinator II will manage subject recruitment, administer study visits, and assist with data analysis while ensuring compliance with study protocols. Key responsibilities...Part timeDataDaily paidWork at office
- ...Langone Health in New York, NY, seeks a Clinical Research Coordinator for the Oncology division. The CRC... ...patient safety, protocol adherence, data quality, and compliance under PI supervision... ..., and CTO/PI teams to pre-screen, consent, schedule visits, manage biospecimens...Data
- ...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...DataWork at office
$43.68k - $73.92k
...$73,920.00 Position Summary The Clinical Research Coordinator functions as an integral part of the Research Team in clinical... ...protocol requirements, informed consent, and follow-up procedures with potential... ...study guidelines. KPA 4 – Data Management, Documentation &...DataWork at office- ...Clinical Research CoordinatorThe Clinical Research Coordinator assists in the daily activities of... ...obtains informed consent; collects, maintains... ...and records study data. Inputs all information... ...us, you become part of Mount Sinai's... ...challenges of our time — discovering and...DataTraineeshipWork at officeLocal areaShift work
$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- 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 Health System is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and organize study data. This role includes preparing grant applications and coordinating IRB/GCO submissions. The position requires a science...Data
- 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
- ...Morningside is seeking an entry-level Clinical Research Coordinator to conduct and assist in clinical... ...The role involves obtaining informed consent, collecting and organizing study information... ...includes responsibilities such as data maintenance, participant 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
- 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
$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- The Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical research studies... .... Responsibilities include obtaining informed consent, collecting and organizing study data, and assisting with grant applications and IRB...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
- ...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 peer... ...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... ...applications, IRB/GCO documents are submitted. Coordinates protocols and human subject approvals... ...trials. May obtain informed consent under general supervision of the Investigator...Data- Clinical Research Coordinator- McComb, MS ICON plc is a world-leading healthcare intelligence... ...complete clinical trial data, including documentation of... ..., including informed consent forms, case report forms, and... ...accommodation for any part of the application process,...DataFlexible hours
- ...Philadelphia, PA 19107 The Clinical Research Coordinator I will work at site to help... ...to provide the best quality data to the sponsor. The CRC I... ...company goals are achieved on a timely basis. DUTIES &... ...concerns. Conduct patient consent discussions and ensure comprehension...Data
- ...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
$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
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