Entry-Level Clinical Research Coordinator I - Data & Consent
Mount Sinai
Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to help manage daily activities of clinical studies, obtain informed consent, and organize study information. You will assist with grant-related documents, IRB submissions, data entry, subject recruitment, and specimen handling, ensuring adherence to hospital procedures and regulations. This role supports investigators and contributes to a culture of excellence in research and patient care within Mount Sinai's #J-18808-Ljbffr Mount Sinai
- The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data. You will assist in grant preparation, IRB submissions, and ensure compliance with hospital procedures...Data
- Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications, IRB submissions, and regulatory filings. The role...DataEntry level
- ...Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study information,... ...Grants and Contracts Office). You will input data into databases, maintain source...DataEntry levelWork at office
- The Clinical Research Coordinator at Mount Sinai Morningside is an entry-level human subjects researcher responsible for conducting and assisting in... ...This role involves obtaining informed consent, collecting and organizing study data, and supporting regulatory submissions...DataEntry level
- ...Medicine (ICCM) in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and organize study data. You will assist in grant... ...Responsibilities include data collection and entry, screening participants,...DataEntry level
- Mount Sinai is seeking an entry-level Clinical Research Coordinator to support dementia-focused studies among older... .... You will obtain informed consent, screen participants, and conduct bilingual... ...supervision. You will assist with data collection, documentation, and...DataEntry level
$64.35k - $70k
Join to apply for the Clinical Research Coordinator - PACC role at Columbia University... ...limited to recruiting and consenting patients, conducting study... ...source documentation and data entry. Collect, record, and... ...local residents. Seniority level Seniority level Entry level...DataEntry levelFull timeTemporary workWork at officeLocal area- ...Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical... ...collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks... ...supervision. Responsibilities include data entry, participant screening,...DataPart time
- ...Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant-related... ...procedures. Responsibilities include data entry, subject screening, consent...DataHourly payPart time
$66.3k - $68k
...Irving Medical Center is looking for a Clinical Research Coordinator. This position supports clinical... ...coordinating patient participation and data management under direct supervision. The... ...include participant recruitment, data entry, and maintaining research compliance....DataEntry levelWork at office$58.66k - $73.53k
...Sinai are seeking a highly motivated Clinical Research Coordinator I to join a growing, multidisciplinary... ...participants and obtain informed consent under the supervision of study investigators... ...procedures. Coordinate clinical data and biospecimen collection, including...DataEntry levelTraineeshipLocal area- ...limited to: scope of role, level of experience, education, accomplishments... ...Medicine (CRM), the Clinical Research Coordinator will work closely with... ...office setting and the OR, data management activities while... ...and conducts the informed consent process on studies as...DataEntry levelFull timeWork at officeLocal areaFlexible hoursShift work
- About Profound Research Profound Research partners with... ...physicians to offer clinical trials as a therapeuticoptionfor... ...a Clinical Research Coordinator I at Profound Research... ...teams. This is not an entry-level support role -you’llbe... ...-related procedures, data collection, and...DataEntry levelFull timeContract workFor contractorsWork at office
- ...science of dermatology through research and education.From... ...patients through science.The Clinical Research Coordinator is an entry human subjects researcher... ...obtains informed consent, collects, maintains and... ...and review of experimental data for publication and presentation...DataHourly payTraineeshipWork at officeLocal area
$26.77 - $40.05 per hour
...Informed by basic research done at our Sloan... ...translational and clinical research that is driving... ...Clinical Research Coordinator (CRC) to join the... ...management and data management on... ...study enrollment and consent processAssist the... ...preferredExperience using data entry tools like REDCap...DataFull timeMonday to FridayFlexible hoursShift workAfternoon shift- DescriptionThe Parsons Research Center for Psychedelic Healing... ...an opening for a full-time clinical research coordinator to oversee day-to-day operations... ...to: obtaining informed consent, screening participants for... ...and review of experimental data for publication and presentation...DataHourly payFull timeTraineeshipLocal areaRemote work
- ...analyzes and interprets highly complex clinical research data; conducts clinical testing and... ...IRB / GCO documents are submitted.10. Coordinates protocols and human subject approvals... ...trials.12. Independently obtains informed consent for all types of clinical studies and...Data
- ...Description Under minimal supervision coordinates the clinical assessments of the study subjects;... ...moderately complex clinical research data. Prepares grant applications and documents... ...clinical trials. Obtains informed consent under supervision of the Principal Investigator...DataFull timeWork at office
- ...Clinical Research Coordinator I Clinical Research Coordinators (CRCs) are key members... ...study coordination, data collection, regulatory compliance... ...(CRFs). Complete data entry activities with supervision... ...Support recruitment and consenting activities for pharmaceutical...DataWork at officeLocal area
$17 - $38 per hour
...Description The Clinical Research Coordinator Part-time performs all the regular duties of a Clinical... ...clinical research studies obtains informed consent; collects maintains and organizes... ...1. Collects and records study data. Inputs all information into database...DataHourly payPart timeWork at office- ...Clinical Research Coordinator The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and... ...individual obtains informed consent, collects, maintains and organizes... ..., and review of experimental data for publication and...DataHourly payTraineeshipWork at officeLocal area
- ...Description The Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information... ...Collection of study data data entry and maintenance of research databases...DataFull timeWork at office
- Mount Sinai Health System in New York seeks a Clinical Research Coordinator to assist in the daily activities of clinical research studies, obtain informed consent, and organize study information. You will help prepare grant documents, maintain source documents, and support...Entry level
- The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. Responsibilities include data collection, maintaining source documents, assisting with grant...Data
- ...functional project activity within our Clinical Solutions team, coordinating timelines, milestones and... ...accelerate drug development programs. This entry-level PM role offers exposure to global... ...collaboration with clinical operations and data teams, and the chance to contribute...DataEntry level
- ...Make a Difference Through Clinical Research Are you passionate about... ...compassionate Clinical Research Coordinator (CRC) to join our growing... ...requirements. Obtain informed consent and educate participants on... ...and maintain accurate study data and source documentation....DataWork at office
- ...The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing... ...Collects and records study data. Inputs all information into database...DataFull timeTraineeshipWork at officeLocal area
- ...within Mount Sinai's Icahn School of Medicine invites applications for a Clinical Research Coordinator I. Responsibilities include data collection, specimen handling, obtaining informed consent, and maintaining study records under supervision. The role supports clinical...Data
$43.68k
...New York Medical College is seeking a clinical research coordinator to work with our team on multiple... ...well as prospective and retrospective data entry for multiple studies. Category:... ...clinical trial protocols and informed consent forms • Assist Principal and Sub-...DataFull timeContract workWork at office- ...Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of... ...studies, obtain informed consent, and collect, organize, and maintain... ...proper documentation and data integrity. Responsibilities include data entry, participant screening, consent...Data
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