Part-Time Clinical Research Coordinator: Data & Consent
$16.5 - $38.48 per hourMount Sinai Morningside
Mount Sinai Morningside in New York, NY seeks a part-time Clinical Research Coordinator to assist in daily activities of clinical research studies. The role involves collecting and organizing study data, obtaining informed consent from participants, and preparing grant applications. Qualifications include a Bachelor’s degree in a science-related field or relevant research experience. The hourly pay ranges from $16.50 to $38.48, depending on experience and education. #J-18808-Ljbffr
- ...Mount Sinai Medical Center is seeking a part-time Clinical Research Coordinator to perform essential duties related to clinical research... ...studies. Responsibilities include collecting study data, obtaining informed consent, and preparing grant applications. This position...Part timeDataHourly pay
$21 - $35 per hour
...The Mount Sinai Medical Center is seeking a Per Diem Clinical Research Coordinator to assist in various clinical research studies. This individual will handle informed consent, maintain study documents, and perform necessary research activities. A healthcare background...DataHourly payDaily paid$21 - $35 per hour
...Description The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research Coordinator,... ...research studies, obtains informed consent; collects, maintains and... ...and tabulates research data. Obtains informed consent under...Part timeDataHourly payDaily paidFull timeTraineeshipWork at office- ...activities of a clinical trial in... ...Good Clinical Research Practice (GCP).... ...including protocol coordination (screening, recruiting... ..., enrolling, consenting), feasibility planning, data management,... ...compliance in a timely fashion. Maintains... ...full‑time and part‑time colleagues...Part timeDataDaily paidFull timeTemporary workFlexible hoursShift work
- ...Clinical Research Coordinator, Part-time The Clinical Research Coordinator, Part-time performs all the regular... ...research studies, obtains informed consent; collects, maintains and organizes study... ...1. Collects and records study data. Inputs all information into database...Part timeDataHourly payTraineeshipWork at officeLocal areaShift work
- ...Medical Center is seeking a Clinical Trial Manager to... ...accordance with Good Clinical Research Practice (GCP). Responsibilities include coordinating various aspects of... ...trials, managing data, and training staff. The... ...are provided to full-time and part-time employees, including...Part timeDataFull time
$68.4k - $232.8k
## Associate Clinical Project Manager, Sponsor... ...ensures high-quality data delivery and... ...managing informed consent process, managing site... ...Managers are an integral part of clinical trial... ...applicable clinical research regulatory... ...Organization - Planning, time management and prioritization...Part timeDataFull timeContract workLocal areaImmediate startWork from homeWorldwide- ...NYU Langone Health seeks an Associate Clinical Research Coordinator (NT aCRC) to coordinate oncology clinical... ...safety, protocol adherence, and quality data collection across study sites. Responsibilities include screening, consent processes, biospecimen handling, data entry...Data
- ...Responsibilities Conduct and coordinate all aspects of clinical trial activities at the site.... ...regulatory binders, and informed consent forms. Perform timely and accurate data entry into electronic data... ..., monitors, and other research team members. Ensure compliance...DataWork at office
$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$46.5k - $48.5k
...Clinical Research Coordinator A Renal division in the department of medicine... ...compliance, and data quality, requiring adherence... ...recruit, and enroll consenting patients using Good... ...organizational and time‑management skills;... ...demonstrated ability to work as part of a team as well as...DataLocal areaFlexible hours- ...leading healthcare institution in New York is seeking a Clinical Research Coordinator to assist in daily activities of clinical research studies, including collecting and organizing data, obtaining informed consent, and preparing grant applications. This is an entry-...Data
$23 - $26 per hour
...too! Are you passionate about clinical research and patient care? Do you have strong... ...Research team. This is a Full-time position, working hours is... ...such as interviewing subjects, data collection and recording; Obtained informed consent; educated potential study participants...DataFull timeWeekend workAfternoon shift$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$45 - $60 per hour
...Center for Cancer Research (“START”) is the world... ...to oncology clinical research. Throughout... ...Clinical Research Coordinator. The Clinical Research... ...the accurate and timely conduct of... ...patient interaction, data collection, and maintaining... ...the informed consent process ensuring...DataCurrently hiringWork at officeLocal areaMonday to FridayFlexible hours$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- ...St. Luke’s Cancer Institute Research encompasses cancer care for... ...of this position is the coordination of adult clinical trials. A successful candidate... ...and documents informed consent process. Reviews clinical records... ...and extracts necessary data to determine eligibility and...Data
$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$47.31k - $53.42k
...Clinical Research Coordinator A/B (Pregnancy & Perinatal Research Center... ...subject recruitment, data entry, collection of... ...across multiple studies Consenting patients into... ...independently and as part of a team, with strong... ...through TIAA and Vanguard. Time Away from Work:...DataLocal areaFlexible hours$46.5k - $58.06k
...Job Title Clinical Research Coordinator A/B (Department of Cardiology) Job Profile... ...conduct follow-up assessments, data collection and use of EDC... ...within protocol designated time frames; assure research orders... ...and explain protocol and consent forms. Assure original...DataLocal areaFlexible hours$63.65k - $85k
...Under minimal supervision, coordinates the clinical assessments of the study subjects... ...complex clinical research data. Prepares grant applications... ...clinical trials. Obtains informed consent under supervision of the... ...you join us, you become part of Mount Sinai’s unparalleled...DataTraineeshipWork at office$250k
...New York (PAGNY) is adding a Clinical Research Coordinator to the group at NYC Health... ...Events (SAEs), providing timely medical interventions and reporting... .... Conduct the Informed Consent process, ensuring patients... ...(EMR) and Electronic Data Capture (EDC) systems. Exceptional...DataImmediate startFlexible hours$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$47.31k
...Clinical Research Coordinator The Abramson Cancer Center of the University of Pennsylvania... ...The TCE‑TOPP seeks a full‑time Clinical Research... .... Experience screening and consenting patients is required. Prior... ...with abstraction of medical data from EPIC (Penn Chart) is highly...DataFull timeLocal areaFlexible hours$17 - $41.08 per hour
...Job Title: Clinical Research Coordinator – Entry Human Subjects Researcher The Clinical Research Coordinator... .... This individual obtains informed consent, collects, maintains, and organizes... ...analysis, and review of experimental data for publication and presentation. Assist...DataHourly payWork at office- ...Job Description Our clinical research company is looking to hire... ...candidate for the full-time position of Clinical Research Coordinator in our New Jersey location... ...care activities: consenting patients, physical assessments... ...reminder phone calls. Data entry of case report...DataFull timeLocal areaRemote workWeekend work
$52.5k - $67.05k
...Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical... ..., recruitment, consent, and enrollment of study... ...; accurate data collection, entry, and... ...safety reporting in a timely and accurate manner.... ...demonstrated ability to work as part of a team, as well as...DataLocal areaFlexible hours$66.2k - $90k
...minimal supervision, coordinates the clinical assessments of the study... ...complex clinical research data. Prepares grant applications... ...Obtains informed consent under supervision of... ...join us, you become part of Mount Sinai’s unparalleled... ...challenges of our time — discovering and...DataTraineeshipWork at officeLocal area$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... ...Obtain informed consent and assent for adult... ...Perform accurate and timely data entry in sponsor EDC...DataWork at officeRemote work- ...Clinical Research Coordinator * Must Have Experience With Oncology Clinical... ...New York, NY Full-Time/Regular NYU Grossman... ...people. An integral part of NYU Langone Health... ...Coordinators (CRCs), Data Coordinator Unit (DCU... ..., through the consenting process, through the...DataFull time
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