Part-Time Clinical Research Coordinator: Data & Consent
Mount Sinai Morningside
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 is hourly and eligible for overtime for part-time staff, with duties including data management, consent education, and coordination of study materials and regulatory documents. #J-18808-Ljbffr
- 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- ...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... ...1. Collects and records study data. Inputs all information into database...Part timeDataHourly payFull timeTraineeshipWork at officeLocal area
$66.3k
...compensation at the time of posting. Position... ...leadership in scientific research, health and medical... ...students and over 3,000 part-time and full-time... ...research endeavors. Clinical Research Coordinators (CRCs) are key members... ...study coordination, data collection, regulatory...Part timeDataFull timeTemporary workWork at officeLocal area$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... ...activities (i.e., informed consent, screening, and protocol...DataLocal area- DescriptionThe Clinical Research Coordinator is an entry human subjects... ...individual obtains informed consent, collects, maintains... ...of experimental data for publication and presentation... ...join us, you become part of Mount Sinai’s... ...challenges of our time — discovering and...DataHourly payTraineeshipWork at officeLocal 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
- ...Mount Sinai Medical Center is hiring a Clinical Research Coordinator to support clinical research studies by obtaining informed consent and collecting specimens. Ideal candidates should... .... The role is essential for ensuring data accuracy and compliance within the research...DataHourly pay
- ...Columbia University is hiring a full-time Clinical Research Coordinator for the NIH-funded CAMEO study in Crohn... ...coordinate study activities, manage data, and ensure regulatory compliance... ...Responsibilities include participant recruitment, consent, data entry, IRB liaison, and study...DataFull timeFlexible hours
$17 - $41.08 per hour
...Mount Sinai Medical Center is seeking a Clinical Research Coordinator responsible for conducting and assisting in clinical research studies... ...supervision. The role includes obtaining informed consent, collecting data, and assisting in grant applications. The ideal candidate...DataHourly pay$17 - $41.08 per hour
...Mount Sinai Medical Center is seeking a Clinical Research Coordinator in New York, NY. This role involves conducting clinical research studies, obtaining informed consent, and collecting data. Candidates should possess a Bachelor's degree in science or a related field...DataHourly pay- ...Summary We are seeking a Senior Clinical Research Coordinator to lead the day-to-day... ...participant screening, informed consent, visit scheduling, and... ...clinical decision-making. Oversee data entry and query resolution in EDC systems, ensuring timely and accurate data submission...Data
- ...Clinical Research AnalystUnder general supervision, analyzes and interprets... ...complex clinical research data; conducts clinical testing and... ...GCO documents are submitted.Coordinates protocols and human subject... ...Independently obtains informed consent for all types of clinical...Data
- ...Clinical Research Coordinator IIA highly organized and enthusiastic research coordinator (RC) is needed to carry out... ...protocol write-up and submission, informed consent development, completion of appropriate HIPAA Forms and Data Usage Agreements, submission of renewals, modifications...DataLocal area
$52k - $65k
...Yes Department: Urology - Research Work Shift: Day Work Days:... ....00-$65,000.00 Job Summary Clinical Research Coordinator II will oversee multiple clinical... ...training. Screens and consents patients and ensures the scheduling... .... Collects required data and imaging and ensures data...DataShift work$54k - $84k
...Job Description Full time or Part time Join our outstanding team of professionals. We are looking for a Clinical Research Study Coordinator to work as part of our research team. We provide... ...and sponsor) Administering informed consent as delegated by Principle Investigator...Part timeFull timeTemporary workFlexible hours- ...Clinical Research CoordinatorResearch -- AdministrationNew... ...York, NY • Full-Time/RegularNYU... ...people. An integral part of NYU Langone... ...Clinical Research Coordinator. The Oncology Clinical... ...(CRCs), Data Coordinator Unit... ...screening, through the consenting process, through...DataFull time
$58.66k - $80k
...Clinical Research Coordinator IStrength Through DiversityGround breaking science. Advancing... ...studies, obtains informed consent; collects, maintains and... ...Collects and records study data. Inputs all information... ...you join us, you become a part of Mount Sinai's unrivaled...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- ...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
- ...University is a leading research university that... ...Nursing is seeking a Clinical Research Coordinator II to support the day... ...highest standards of data quality, regulatory compliance... ...eligibility and consents study participants... ...advance to allow adequate time for coordination. #J-...DataRemote workWork from home
$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$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- ...Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting... .... This individual obtains informed consent, collects, maintains and organizes... ...analysis, and review of experimental data for publication and presentation....DataHourly payTraineeshipWork at office
- ...an alternative application process. Clinical Research Coordinator Full Time Staten Island, NY, US 3 days ago Requisition... ...Review and obtain informed consent from with potential study volunteer... ...studies in manner to ensure integrity of data and safety of subjects. Enter data...DataFull timeWork at office
- ...Clinical Research CoordinatorUnder minimal supervision, coordinates the clinical assessments of the study... ...research data. Prepares grant applications... ...Obtains informed consent under supervision... ...us, you become part of Mount Sinai's... ...of our time — discovering and...DataTraineeshipWork at officeLocal areaShift work
$25 - $36 per hour
...About Us Flourish Research is where clinical trials thrive.Flourish... ...a Clinical Research Coordinator to supportour Philadelphiasite... ...and study data per regs/GCP; maintain... ...eCRFs. Obtain informed consent per federal regs, GCP... ...duties safely, and in a time-/cost-effective...DataHourly payWork at officeMonday to FridayShift work$44.85k - $54.6k
...Classification Title Clinical Research Associate I (Non-exempt... ...I (Clinical Research Coordinator) performs a vital role... ...research studies at any time. This position reports... ...and quantitative data and data collection forms... ...including obtaining informed consents and screening subjects...DataWork at office$36 - $48 per hour
..., longitudinal multi-omics data in clinical context to deeply profile the... ...a remote contract Clinical Research Coordinator to execute and coordinate... ...operations—from recruitment and e‑consent to virtual follow‑up and... ...world data. This is a full‑time remote contract role (40...DataHourly payFull timeContract workFor contractorsRemote work- ...Clinical Research Coordinator The Department of Pediatrics is seeking a full-time Clinical Research Coordinator to join our team working... ...with PI. Participate in the consent/assent process ensuring the... ...key personnel including the Data Coordinating Center at Connecticut...DataFull timeLocal areaImmediate startFlexible hours
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