Part-Time Clinical Research Coordinator — Data & Consent Expert
Mount Sinai Health System
Mount Sinai Health System is seeking a part-time Clinical Research Coordinator in New York City. The position involves assisting in daily activities of clinical research studies, including obtaining informed consent and organizing study information. This role is hourly and eligible for overtime, requiring a Bachelor's degree in science or a relevant combination of experience and education. Responsibilities include data collection, participant education, and preparation of grant applications. #J-18808-Ljbffr Mount Sinai Health System
$16.5 - $39.88 per hour
Mount Sinai Health System seeks a part-time Clinical Research Coordinator in New York City. This role includes collecting and managing study data, obtaining informed consent from participants, and assisting with grant applications. Candidates should have a Bachelor's degree...Part timeHourly pay$16.5 - $39.88 per hour
Mount Sinai Morningside is looking for a Part-time Clinical Research Coordinator in New York, NY. This role involves supporting clinical research studies by collecting and maintaining data, obtaining informed consent, and assisting with grant applications. Ideal candidates...Part timeHourly pay- ...Community Care seeks a Research Coordinator to oversee study... ...include obtaining informed consent, conducting research assessments... ...managing participant data. The ideal candidate... ...skills, and prior clinical research experience.... ...role plays a crucial part in assisting with the...Suggested
$16.5 - $39.88 per hour
Mount Sinai Medical Center is looking for a part-time Clinical Research Coordinator to assist in daily activities of clinical research studies. This role involves collecting study data, obtaining informed consent, and preparing grant applications. Applicants should preferably...Part timeHourly pay- ...looking for an administrator to help coordinate human subjects studies. The... .... Responsibilities: Overseeing research sessions Explaining procedures and obtaining consent from participants Operating the... ...studies are stocked This is a part-time position, which will require...Part timeWork at office2 days per week1 day per week
- 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. Inputs all information into database...Part timeHourly payTraineeshipWork at office
- Overview We are seeking a Certified Clinical Research Coordinator (CCRC) to join our growing clinical research site on a part-time basis (one day per week) . This role is ideal... ...including participant screening, informed consent, visit coordination, and protocol-specified...Part timeHourly payExtra incomeFull time1 day per week
$16.5 - $39.88 per hour
Mount Sinai Health System is hiring a part-time Clinical Research Coordinator in New York City. This role involves collecting and recording study data, obtaining informed consent from participants, and assisting with grant applications and research protocols. Candidates...Part timeHourly pay- A clinical research facility in New York is looking for a Certified Clinical Research Coordinator (CCRC) to join part-time, one day per week. The role involves coordinating clinical trials, ensuring compliance with regulations, and maintaining participant relations in...Part timeHourly payFlexible hours1 day per week
$33.67 - $40.97 per hour
NYU Langone Hospitals in New York City is seeking a part-time Research Coordinator to oversee and coordinate research studies at the Medical Center... ...as recruitment, grant submissions, and compliance with clinical regulations. The ideal candidate will possess a Bachelor'...Part timeHourly payWork at office$67k - $69k
...compensation at the time of posting. Position... ...leadership in scientific research, health and medical... ...and over 3,000 part‑time and full‑time faculty... ...research endeavors. Clinical Research Coordinators (CRCs) are key members... ...study coordination, data collection, regulatory...Part timeFull timeTemporary workWork at officeLocal area- ProPharma Group is looking for a Lead Clinical Research Coordinator to manage clinical trial activities in New York. Responsibilities include overseeing... ...in both English and Spanish. The position offers part-time hours within a remote working environment. #J-18808-Ljbffr...Part timeRemote job
- ...new solution in the clinical trials space. Our client... .../English) Clinical Research Coordinator to play a central... ...partners. Strong time-management and prioritization... ..., and informed consent processes when authorized... ...and electronic data entries. Monitor participant...Work at officeWork from home1 day per week
$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...Hourly payFull timeContract workFor contractorsRemote work- ...Position Summary Travel Clinical Research Coordinator plays a key role in supporting... ...close out Recruit, screen, consent, and enroll participants according... ...document accurate study data including source... ...adverse event reports Ensure timely and accurate electronic data...Night shiftAfternoon shift
- ...instant access to expert neurologists, cutting... ...wraparound care coordination and behavioral health... ...About the Role: The Clinical Research Coordinator (CRC)... ..., and enters study data accurately and in a timely manner using electronic... ...supports informed consent discussions,...Remote workWork from home
$43 - $46 per hour
...Job Title: Clinical Research Coordinator Location: New York, NY 10021 Type: Contract... ...accuracy of human subject data. This role involves working... ...information Support recruitment, consent, and data collection for... ...or reporting Provide real-time updates on data entry and...Hourly payContract workWork at officeMonday to Friday$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...Hourly payFull timeContract workRemote work- ...lifelong health. This is a full-time, remote position for a Research Coordinator to support the Clinical Research Team, coordinating... ...protocol. Coordinate transfer of data between Omada and... ...at a basic level with informed consent, protocols, and IRB requirements...Full timeRemote workWork from homeFlexible hours
- ...Clinical Research Coordinator The position is responsible for collaborating with... ...organizational, multi-tasking, time management, communication,... ...parent-reporting outcomes data. Identifying and... ...Participate in the informed consent process and Randomizing participants...Local area
- ...Job Title Clinical Research Coordinator Job Description Under... ...complex clinical research data. Prepares grant... ...Obtains informed consent under supervision of... ...join us, you become part of Mount Sinai's unparalleled... ...care challenges of our time discovering and...Full timeTraineeshipWork at officeLocal areaShift work
- ...Clinical Research Coordinator - Cardiology The Clinical Research Coordinator (CRC) will support investigator... ...manager, a biostatistician, and a data manager to execute high-quality... ...eligibility and coordinate informed consent per IRB-approved protocols. Schedule...Local area
$56k - $71k
...Research Coordinator Works as research coordinator providing support necessary... ...the operation of ongoing clinical trials in the Department of... ...person and virtually Infonned consent process Study subject... ...(CRFs; eCRFs) and other data collection tools as requested...- ...Clinical Research Coordinator The Clinical Research Coordinator assists... ..., obtains informed consent; collects, maintains... ...Collects and records study data. Inputs all... ...join us, you become part of Mount Sinai's unparalleled... ...challenges of our time discovering and applying...Full timeTraineeshipWork at officeLocal areaShift work
- ...Clinical Research Coordinator Under minimal supervision, coordinates... ...complex clinical research data. Prepares grant... .... Obtain informed consent in compliance with institutional... ...accurate and timely study records, logs,... ...independently as well as part of a team....Full timeTraineeshipWork at officeLocal areaShift work
$58.66k - $73.53k
Mount Sinai Health System is seeking a Clinical Research Coordinator in New York City. This role involves assisting in the daily activities of clinical research studies, including obtaining informed consent and maintaining study information. A Bachelors or Masters degree...$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...Work at office$58.66k - $73.53k
Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists... ...participants Collection of study data, data entry, and maintenance of research...TraineeshipWork at office$58.66k - $73.53k
Mount Sinai Morningside in New York is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research... ...studies. Responsibilities include collecting study data, obtaining informed consent, and assisting in grant application preparation. A...$66.2k - $90k
Job Description A Clinical Research Coordinator (CRC) II position is currently available... .... Duties will include data collection and management of... ...patient clinical information, timely collection of protocol... ...required, obtain informed consent, collect, maintain and organize...TraineeshipWork at officeLocal area
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