Part-Time Clinical Research Coordinator: Consent & Data
Mount Sinai Morningside
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 facility. The role involves assisting in grant preparation, maintaining study files, coordinating with IRB submissions, and ensuring compliance and accurate documentation while supporting study participants and staff. #J-18808-Ljbffr 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...Part timeDataHourly pay
- 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
- Mount Sinai Health System in New York is seeking a part-time Clinical Research Coordinator to support ongoing studies. The role involves... ...daily study activities, obtaining informed consent, collecting and organizing data, and assisting with grant documentation. Responsibilities...Part timeData
- 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...Part timeDataHourly pay
$24 - $43 per hour
...Optum NY/NJ, is seeking a Part -Time Clinical Research Coordinator to join our team in Mount Kisco, NY. Optum is... ...you'll have the clinical resources, data and support of a global organization... ...out administrative procedures for the consent, enrolling and randomization process...Part timeDataHourly payMinimum wageFull timeTemporary workWork experience placementLive inWork at officeLocal areaWork from homeMonday to Friday- ...Clinical Research Coordinator II Columbia University Irving Medical Center (CUIMC) provides global leadership... ...4,472 students and over 3,000 part-time and full-time faculty members, the... ...and tasks include study coordination, data collection, regulatory compliance, and...Part timeDataFull timeWork 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
$36 - $48 per hour
...biotechnology company is looking for a remote Clinical Research Coordinator to manage decentralized clinical... ...on autoimmune studies. This full-time contract position requires a... ..., conducting virtual informed consent, and managing data collection. The role offers a competitive...DataHourly payFull timeContract workRemote work- ...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
- ...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... ...submission, informed consent development,... ...appropriate HIPAA Forms and Data Usage Agreements, submission...DataTemporary workLocal area
- ...an alternative application process. Clinical Research Coordinator Full Time Staten Island, NY, US About Company:... ...Investigator Review and obtain informed consent from with potential study volunteer... ...in manner to ensure integrity of data and safety of subjects. Enter data as...DataFull timeWork at office
$30 - $33 per hour
...Description *URGENT NEED - Clinical Research Coordinator Responsibilities Lead and coordinate... ...Committee (HROC), data collection plans, and finance... ...that IRB-approved informed consent is obtained, properly... ...accurate. Provide accurate, timely, and well-supported responses...DataContract workTemporary work- ...Clinical Research CoordinatorThe Department of Pediatrics is seeking a full-time Clinical Research Coordinator to join our team working on a National Institutes... ...PI.Participate in the consent/assent process ensuring... ...personnel including the Data Coordinating Center at Connecticut...DataFull timeLocal areaImmediate startFlexible hours
$70.48k - $74.79k
...people. An integral part of NYU Langone... ..., scientific research, and direct patient... ...our team as a Clinical Research Coordinator. The Oncology Clinical... ...(CRCs), Data Coordinator Unit... ...screening, through the consenting process, through... ...and ensuring a timely, accurate and...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 area
- ...Senior Clinical Research CoordinatorNYU Grossman School of... ...people. An integral part of NYU Langone Health... ...Senior Clinical Research Coordinator. The Senior Clinical... ...efficiently.Obtain informed consent and assent for adult... ...Perform accurate and timely data entry in sponsor EDC...DataWork at officeRemote work
$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... ...and signature. Perform accurate and timely data entry in sponsor EDC systems and...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... ...required, obtain informed consent, collect, maintain... ...join us, you become part of Mount Sinai's...DataTraineeshipWork at officeLocal areaShift work
- ...Job Description The Clinical Research Coordinator is an entry human... ...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
- ...Clinical Research Analyst Under general supervision, analyzes and interprets... ...complex clinical research data; conducts clinical testing... ...documents are submitted. Coordinates protocols and human subject... ...Independently obtains informed consent for all types of clinical...Data
- ...Sinai Health System in New York seeks an entry-level Clinical Research Coordinator to conduct and assist in human subjects research... ...research staff. You will obtain informed consent, collect and organize study data, and help prepare grant-related documents. Responsibilities...Data
- ...Intermediate LLC, doing business as Tandem Clinical Research, seeks a detail-oriented Clinical Research Coordinator to support clinical trials in Healthcare... ...participant recruitment, informed consent, study visits, and data collection while ensuring strict adherence...Data
- Columbia University is seeking an entry-level Clinical Research Coordinator to support Cardiology research under supervision. The role involves data entry in EDC/RedCap/CTMS, basic data... ..., scheduling visits, processing consents, and assisting with study initiation, audits...Data
- ...Morningside in New York City seeks a Clinical Research Coordinator for the KPMP and Renal Biorepository... ..., retention, biospecimen processing, data entry, and collaboration with investigators... ...prescreening with Epic EMR, informed consent during Enrollment Visits,...Data
- ...Center is seeking a Clinical Research Coordinator II for the Tisch Cancer... ...The role focuses on data collection and management... ...information, with timely shipment of protocol-... ...obtaining informed consent under supervision. The... ...Tisch Cancer Center, part of Mount Sinai Health...Data
- Flourish Research is seeking a Clinical Research Coordinator for our Philadelphia site. The role involves coordinating protocol... ..., and injections, while ensuring data quality and regulatory compliance.... ...patients and manage informed consent under IRB and FDA/GCP guidelines....Data
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Part-Time Clinical Research Coordinator: Consent & Data. Be the first to apply!


