Part-Time Clinical Research Coordinator Data & Consent Expert
Internal Medicine
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
$16.5 - $39.88 per hour
...Sinai Medical Center in New York, NY, is seeking a part-time Clinical Research Coordinator who performs various duties related to clinical... ...Responsibilities include collecting and recording study data, obtaining informed consent, assisting in the screening and registering of...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- ...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 timeHourly pay
$58.66k - $73.53k
...Job Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.... ...Responsibilities Collects and records study data. Inputs all information into database...SuggestedTraineeshipWork at office$58.66k - $73.53k
...Mount Sinai Medical Center is seeking a Clinical Research Coordinator to assist in daily activities for clinical research studies, including collecting data and obtaining informed consent. The ideal candidate will have a Bachelor’s or Master’s degree in a Science-related...Suggested$21 - $35 per hour
...Job Description The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research... ...research studies, obtains informed consent; collects, maintains and organizes... ...and tabulates research data. Obtains informed consent under...Part timeHourly payDaily paidFull timeTraineeshipWork at office- ...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
- ...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
- ...Description The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research... ...research studies, obtains informed consent; collects, maintains and organizes study... ...Collects and records study data. Inputs all information into database...Part timeHourly payTraineeshipWork at officeLocal area
$21 - $35 per hour
...Per Diem Clinical Research Coordinator The Per Diem Clinical Research Coordinator... ...regular duties of a full or part time Clinical Research... ...studies, obtains informed consent; collects, maintains and organizes... ...Collates and tabulates research data. 2. Obtains informed...Part timeHourly payDaily paidFull timeTraineeshipWork at officeLocal areaShift work$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- ...highly organized administrator to coordinate human subjects studies. The role involves overseeing research sessions, explaining procedures and obtaining consent, operating the study-site... ...maintaining organized files. This part-time position requires presence in the...Part timeWork at office2 days per week1 day per week
- ...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
$67k - $69k
...compensation at the time of posting. Position... ...leadership in scientific research, health and medical... ...students and over 3,000 part‑time and full‑time... ...research endeavors. Clinical Research Coordinators (CRCs) are key members... ...study coordination, data collection, regulatory...Part timeFull timeTemporary workWork at officeLocal area- ...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
- ...will contribute your expertise to a cutting-edge project involving state-of-the-art large language models and help create high-quality data essential for AI innovation. The role starts in April with rolling applications and requires 15-20 hours of work per week, with...Part time
$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. Benefits...Immediate startFlexible hours- ...Spanish-speaking Clinical Research Coordinator We’re hiring: Clinical Research Coordinator (Spanish-speaking). To apply: Send your CV and letter... ...Conduct participant recruitment, screening, and informed consent procedures Perform blood draws and other study-related sample...Local area
$70k - $100k
...all. With hundreds of research locations, mobile clinics, and clinicians... ...Travel Clinical Research Coordinator primary... ...adequate preparation and time for interaction during... ...appointment Obtain informed consent per Care Access SOP... ...: Record data legibly, in real time...Full timeTemporary workLocal areaWorldwideVisa sponsorshipWork visaFlexible hours- ...Job Description The Clinical Research Coordinator is an entry human subjects... ...obtains informed consent, collects, maintains... ...review of experimental data for publication and... ...join us, you become part of Mount Sinai’s unparalleled... ...challenges of our time — discovering and...Hourly payTraineeshipWork at officeLocal area
$60k - $70k
...Sites across the research and clinical trials landscape.... ...Clinical Research Coordinator (CRC) to join Vitalief as a full‑time employee with comprehensive... ..., New Jersey, as part of a large... ...Identify, screen, and consent eligible patients... ...maintain study data in source documents...Full timeTemporary workWork at officeMonday to Friday- ...Job Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for... ...staff. This individual obtains informed consent, collects, maintains and organizes... ...analysis and review of experimental data for publication and presentation. Maintains...Hourly payWork at office
$66.2k - $90k
...Description Under minimal supervision, coordinates the clinical assessments of the study subjects;... ...interpreting moderately complex clinical research data. Prepares grant applications and... ...ongoing clinical trials. Obtains informed consent under supervision of the Principal...TraineeshipWork at office- ...Mount Sinai Medical Center in New York is seeking a Clinical Research Coordinator to assist in clinical research studies. This entry-... ...human subjects research, obtaining informed consent, and ensuring accurate data collection. Candidates should have a Bachelor's degree...Hourly pay
$58.66k - $73.53k
...prominent medical institution in New York is looking for a Clinical Research Coordinator to assist with daily clinical research activities, including collecting and organizing study data, obtaining informed consent from participants, and preparing necessary grant...- ...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-...
$21 - $35 per hour
...Sinai Health System in New York is hiring a Per Diem Clinical Research Coordinator. This position involves performing duties as needed... ...research studies including obtaining informed consent and maintaining study data. The ideal candidate should have a health care background...Hourly payDaily paid$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$17 - $41.08 per hour
...Mount Sinai Morningside in New York is looking for a Clinical Research Coordinator – Entry Human Subjects Researcher. This role... ...assisting in clinical research studies, obtaining informed consent, and ensuring accurate data compilation. Candidates should have a Bachelor’s...Hourly pay$58.66k - $73.53k
...Mount Sinai Medical Center in New York is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research studies. You will obtain informed consent, maintain study information, and assist in grant applications and other documentation. The...
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