Clinical Research Coordinator I - Data & Consent Support
Mount Sinai Medical Center
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 a Bachelor's or Master's in science or related field; no experience is required, though one year of research experience is preferred. The position is in New York City with salary range shown. #J-18808-Ljbffr Mount Sinai Medical Center
- ...Health System in New York invites applications for a Clinical Research Coordinator I. This entry-level role supports daily study activities, assists in obtaining informed consent, and helps organize and maintain study data across multiple ongoing trials. Responsibilities...Data
- DescriptionThe Clinical Research Coordinator (CRC) is an entry human subjects researcher... ...to: obtaining informed consent, screening participants for... ...and review of experimental data for publication and presentation... ...inclusive practices, and supports the success of every...DataHourly payTraineeshipLocal area
- ...an immediate opening for a Clinical Research Coordinator who will work with human specimens... ..., obtaining informed consent, collecting, maintaining... ...and complete compilation of data.Enters relevant clinical information... ...inclusive practices, and supports the success of every...DataHourly payTraineeshipWork at officeLocal areaImmediate start
- DescriptionThe Parsons Research Center for... ...opening for a full-time clinical research coordinator to oversee day-to-day... ...opportunity to take on support staff roles at training... ...: obtaining informed consent, screening participants... ...review of experimental data for publication and...DataHourly payFull timeTraineeshipLocal areaRemote work
- ...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
$56k - $71k
...trauma center. Maimonides' clinical programs rank among the... .... Overview Works as research coordinator providing support necessary for the operation... ...and virtually Infonned consent process Study subject enrollment... ...(CRFs; eCRFs) and other data collection tools as...DataFull time$66.3k - $68.3k
...posting. Position Summary The Clinical Research Coordinator (CRC) will support investigator-initiated trials (... ...manager, a biostatistician, and a data manager to execute high-quality academic... ...and coordinate informed consent per IRB-approved protocols. Schedule...DataFull timeTemporary workLocal area$58.66k - $80k
...Clinical Research Coordinator IGround breaking science. Advancing medicine. Healing made personal.The Mount... ...research studies, obtains informed consent; collects, maintains and organizes... ...Contracts Office).Collects and records study data. Inputs all information into...DataWork at office- ...Job TitleClinical Research CoordinatorJob DescriptionUnder... ...minimal supervision, coordinates the clinical assessments of the... ...clinical research data. Prepares grant... ...trials.Obtains informed consent under supervision of... ...inclusive practices, and supports the success of every...DataTraineeshipWork at officeLocal areaShift work
- ...The Clinical Research Coordinator assists in the daily activities of clinical research... ...studies, obtains informed consent; collects, maintains and... ...Collects and records study data. Inputs all information into... ...promotes inclusive practices, and supports the success of every...DataFull timeTraineeshipWork at officeLocal area
$58.66k - $73.53k
...Description A Clinical Research Coordinator (CRC) I position is currently available... ...such as, but no limited to, data collection, specimen collection, obtaining informed consent, and maintaining and... ...promotes inclusive practices, and supports the success of every...DataTraineeshipLocal area- ...interprets highly complex clinical research data; conducts clinical testing... ...documents are submitted. Coordinates protocols and human subject... ...trials. May obtain informed consent under general supervision... ...inclusive practices, and supports the success of every individual...DataFull timeTraineeshipLocal area
$66.2k - $98k
...articulated program in epidemiologic research that connects to clinical, basic, and applied... ...operation of research and data collection activities Consent, instruct, and coordinate research participants as... ...the development of grants to support the PIs by conducting literature...DataFull timeTraineeshipLocal area$35 - $42 per hour
...seeking an experienced Sr Clinical Research Coordinator (Sr. CRC) - ONCOLOGY to... ...growing clinical research team supporting a diverse portfolio of... ...activities Screen, recruit, consent, and enroll study... ...expenses Review and resolve data queries within electronic data...DataContract workTemporary work$72.88k - $116.69k
...interprets highly complex clinical research data; conducts clinical testing... ...documents are submitted. Coordinates protocols and human subject... ...trials. May obtain informed consent under general supervision... ...inclusive practices, and supports the success of every individual...DataTraineeshipLocal area$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... ...regulatory binders. Support IRB submissions, amendments...DataHourly payFull timeContract workFor contractorsRemote work$69.5k - $72.5k
...Position Summary The Clinical Research Coordinator I is an intermediate level... ...registries, retrospective data reviews, studies in long-term... ...IND studies. Responsible for consent, screening for eligibility... ...Provides other administrative support for study activity...DataFull timeTemporary workLocal area$70.48k - $74.79k
...education, scientific research, and direct patient... ...join our team as a Clinical Research Coordinator. The Oncology Clinical... ...(CRCs), Data Coordinator Unit (DCU... ...24 business hours. Supports the training and mentorship... ...screening, through the consenting process, through the...DataFull timeWork at office$70.48k - $88.24k
...education, scientific research, and direct patient... ...team as a Senior Clinical Research Coordinator. The Senior Clinical... ...initiated, foundation-supported, and unfunded studies... ...Obtain informed consent and assent for adult... ...accurate and timely data entry in sponsor EDC...DataFull timeWork at officeRemote work- ...seeking a highly motivated Clinical Research Coordinator II (CRC II) to join our growing... ..., regulatory affairs, data management, patient-facing... ...TCI and its Cancer Research Support Unit (CRSU) to provide the... ...criteria. Obtain informed consent under investigator supervision...DataFull timeTraineeshipWork at officeLocal area
- ...Associate Clinical Research CoordinatorResearch -- AdministrationNew... ...Clinical Research Coordinator. The Non-therapeutic... ...biospecimen and data collection. The NT aCRC... ..., and sponsors in support of the clinical trials... ...from pre-screening, consenting, through the screening...DataFull time
- Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant applications. The role involves collaborating with investigators and research...Data
- Mount Sinai Health System seeks a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data with meticulous attention to regulatory requirements. The role also assists in preparing grant documentation and coordinating...Data
$17 - $41.08 per hour
A healthcare institution in New York seeks a Clinical Research Coordinator to conduct human subjects research under supervision... ...-level position involves obtaining informed consent, screening participants, and maintaining study data. Ideal candidates should have a Bachelor’s...DataHourly pay- ...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
- Mount Sinai Morningside seeks a Clinical Research Coordinator in the Dermatology Department to support daily activities of clinical studies, obtain informed consent, and maintain study data. The role involves preparing grant applications and coordinating IRB submissions...Data
- Mount Sinai Medical Center in New York seeks a Clinical Research Coordinator to manage and assist in clinical trials. The role involves... ...This entry-level position is crucial for ensuring data accuracy and patient consent. The salary ranges from $17 to $41.0783 per hour,...DataHourly pay
- 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
$58.66k - $73.53k
Mount Sinai Medical Center is seeking a Clinical Research Coordinator (CRC) I at the Tisch Cancer Center in New York City. This role involves data and specimen collection, obtaining informed consent, and supporting clinical trials. Qualifications include a Bachelor's or...Data- ...Sinai Morningside is seeking a Clinical Research Coordinator to assist in the daily activities... ...studies, obtain informed consent, and collect, maintain and organize... ...Grants and Contracts Office), input data, manage source documents, and support monitoring visits while...DataWork at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator I - Data & Consent Support. Be the first to apply!
- clinical project manager New York, NY
- clinical research coordinator New York, NY
- entry level clinical research coordinator New York, NY
- sr. clinical trial manager New York, NY
- clinical research coordinator ii New York, NY
- temporary clinical research coordinator New York, NY
- neuroscience clinical research coordinator New York, NY
- senior clinical trials manager New York, NY
- clinical research coordinator remote New York, NY
- remote clinical trial manager New York, NY


