Part-Time Clinical Research Coordinator | Data & IRB Prep
Mount Sinai Medical Center
The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage data collection and documentation in accordance with hospital procedures. This hourly position may involve overtime and requires completing tasks such as grant-related documentation, IRB submissions, and coordinating specimen shipments as per protocol. #J-18808-Ljbffr Mount Sinai Medical Center
- ...Clinical Research Coordinator II Columbia University Irving Medical Center (CUIMC... ...72 students and over 3,000 part-time and full-time faculty members... ...study coordination, data collection, regulatory compliance... ..., HIPAA, Columbia IRB and other institutional or...Part timeDataFull timeWork at officeLocal area
$16.5 - $38.48 per hour
Description The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator... ...Collects and records study data and inputs all information into the... ...in preparing grant applications and IRB/GCO for submission and filings. Maintains...Part timeDataHourly payTraineeshipWork at office- ...The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator... ...Responsibilities 1. Collects and records study data. Inputs all information into... ...in preparing grant applications, IRB/GCO for submission and filings. 5....Part timeDataHourly payFull timeTraineeshipWork at officeLocal area
- Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, and collect data for research protocols at our New York... ...study files, coordinating with IRB submissions, and ensuring compliance...Part timeData
- ...Health System in New York is seeking a part-time Clinical Research Coordinator to support ongoing studies. The role... ...consent, collecting and organizing data, and assisting with grant... ...data entry into databases, preparing IRB/GCO submissions, maintaining source...Part timeData
- Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily clinical research activities in New York. The role involves obtaining informed consent, collecting data, and assisting with study logistics and grant-related filings. The position...Part timeDataHourly pay
$23 per hour
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...We are hiring immediately for a full time PREP COOK position. Location : Kirkland &... ...Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or... ...fantastic benefits. Both full-time and part-time positions offer the following benefits...Part timeDataHourly payFull timeLocal areaImmediate startRemote workFlexible hours$24.5 per hour
...New York Law School We are hiring immediately for full time and part time PREP COOK positions. Address : 185 West Broadway, 5th Floor,... ...jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help....Part timeDataHourly payFull timeTemporary workSummer holidayLocal areaImmediate startRemote workFlexible hours$20 per hour
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...Optum NY/NJ, is seeking a Part -Time Clinical Research Coordinator to join our team in Mount Kisco, NY. Optum is a clinician-led care organization that... ...everyone. At Optum, you'll have the clinical resources, data and support of a global organization behind you so you...Part timeDataHourly payMinimum wageFull timeTemporary workWork experience placementLive inWork at officeLocal areaWork from homeMonday to Friday$20 - $29.08 per hour
...comSummarized Purpose: Study coordinator to support ongoing large clinical study in US. Completes... ...required to capture all data as specified by a study protocol... .... Interacts with the research site team and other... ...site staff. * Ensures that IRB approval is obtained prior...DataLocal area- ...- Remote job at Achieve Test Prep. New Jersey. Achieve Test Prep... ...? FLEXIBILITY: Choose full-time or part-time based on your schedule.... ...minimal supervision. Manage data entry, including creating leads... ...stages effectively. Conduct research, analyze findings, and...Part timeDataRemote jobFull timeWork from homeHome officeFlexible hours
- ...diagnostic, treatment, and research services. The Clinical Research Coordinator (CRC) supports the... ..., scheduling, data management, and... ...completion, and ensure timely data entry and... ...Prepare and submit IRB/ethics applications... ...independently and as part of a team. Strong problem...DataWork at office
- ...possible compensation at the time of posting. Position... ...and enthusiastic research coordinator (RC) is needed to carry out and oversee clinical research studies for the... ...Institutional Review Board (IRB) protocol write-up and... ...HIPAA Forms and Data Usage Agreements, submission...DataTemporary workLocal area
$66.3k
...compensation at the time of posting.... ...leadership in scientific research, health and... ...Investigator and/or Clinical Research Manager,... ...Clinical Research Coordinator (CRC) supports the... ...study procedures, and data collection activities... ...GCP, HIPAA, and IRB processes....DataTemporary workWork at officeLocal area$30 - $33 per hour
...Job Description *URGENT NEED - Clinical Research Coordinator Responsibilities Lead and... ...Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance... ...accurate. Provide accurate, timely, and well-supported responses...DataContract workTemporary work- ...an alternative application process. Clinical Research Coordinator Full Time Staten Island, NY, US About Company:... ...appropriate Institutional Review Boards (IRBs) and other outside regulatory... ...studies in manner to ensure integrity of data and safety of subjects. Enter data...DataFull timeWork at office
- ...Clinical Research CoordinatorThe Clinical Research Coordinator assists in the daily activities of... ...and records study data. Inputs all information... ...applications, IRB/GCO for submission... ...join us, you become part of Mount Sinai's... ...challenges of our time — discovering and...DataTraineeshipWork at officeLocal area
- ...Senior Clinical Research CoordinatorNYU Grossman School of... ...people. An integral part of NYU Langone Health... ...Senior Clinical Research Coordinator. The Senior Clinical... ...Prepare and manage all IRB submissions,... ...Perform accurate and timely data entry in sponsor EDC...DataWork at officeRemote work
- ...Clinical Research Coordinator I Columbia University Irving Medical Center (CUIMC)... ...in the Clinical Protocol & Data Management office in the Herbert... ...procedures necessary for timely and complete data management... ...guidelines, HIPAA, Columbia IRB and other institutional or federal...DataWork at officeLocal areaFlexible hours
$70.48k - $74.79k
...people. An integral part of NYU Langone... ...education, scientific research, and direct... ...join our team as a Clinical Research Coordinator. The Oncology... ...Coordinators (CRCs), Data Coordinator Unit... ...policies and ensuring a timely, accurate and... ..., the use of the IRB, study related...DataWork at office- ...Clinical Research CoordinatorThe Department of Pediatrics is seeking a full-time Clinical Research Coordinator to join our team working on a National Institutes... ...personnel including the Data Coordinating Center at Connecticut... ...methods.Oversee IRB communications and all regulatory...DataFull timeLocal areaImmediate startFlexible hours
$70.48k - $88.24k
...Position Summary Senior Clinical Research Coordinator (Senior CRC) at NYU Grossman School of Medicine for... ...as requested. Prepare and manage all IRB submissions, including initial... ...and signature. Perform accurate and timely data entry in sponsor EDC systems and investigator...DataWork at officeRemote work- ...Clinical Research Coordinator (CRC) IIA Clinical Research Coordinator (... ...include activities such as data collection and... ...clinical information, timely collection of protocol... ...Institutional Review Board (IRB) SOPs, sponsor... ...join us, you become part of Mount Sinai's unparalleled...DataTraineeshipWork at officeLocal areaShift work
- ...Clinical Research Analyst Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols... ...ensure grant applications, IRB / GCO documents are submitted. Coordinates protocols and human...Data
- ...Irving Medical Center in New York seeks a Clinical Research Coordinator I for the Pediatric Neuro Muscular... ...subject recruitment, ensure compliance with IRB and CTSC policies, and support study... ...with sponsors and monitors, data entry in EDC systems, and contributing...Data
- HSS is seeking a Clinical Research Coordinator to support the Center for Regenerative Medicine. The role involves coordinating clinical... .... The CRC will liaise with management, sponsors, and clinical staff, manage data collection, and oversee IRB #J-18808-Ljbffr hssData
- ...Morningside in New York seeks a Clinical Research Coordinator to support daily activities... ...consent, and organize study data. You will input information... ...grant documents and IRB submissions, and help ensure... ...screening, data collection, prep for monitoring visits, and handling...Data
- ...Center in New York seeks a highly organized Research Coordinator to oversee clinical studies at the Weinberg Family Cerebral Palsy... ...with precision. Responsibilities include IRB protocol preparation, consent development, data management, subject recruitment, and collaboration...Data
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