Clinical Research Coordinator I: Participant Consent & Data
Mount Sinai Medical Center
Mount Sinai Health System seeks a Clinical Research Coordinator I to assist in daily clinical research activities, obtain informed consent, and support data collection and specimen processing. You will help prepare IRB and grants documents and participate in study-related tasks across a major NIH initiative. You will collect, organize, and maintain study information, coordinate visits, and contribute to data accuracy and regulatory compliance in a fast-paced environment. #J-18808-Ljbffr Mount Sinai Medical Center
- ...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... ...Responsibilities include data entry, participant screening, credentialing for...DataPart time
- 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
- Mount 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 documents under supervision. This hourly role qualifies for overtime as needed...DataHourly payPart time
- ...Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of... ...studies, obtain informed consent, collect and organize study data, and assist in preparing grant... ...collection and entry, screening participants for eligibility, coordinating with...DataWork at office
$43.68k - $73.92k
...0.00 Position Summary The Clinical Research Coordinator functions as an integral part... ...Review Board (IRB). Participates in study site initiation activities... ...requirements, informed consent, and follow-up procedures... ...study guidelines. KPA 4 – Data Management, Documentation...DataWork at office- ...Clinical Research CoordinatorThe Clinical Research Coordinator assists in the daily activities of clinical... ...studies, obtains informed consent; collects, maintains... ...and records study data. Inputs all information... ...investigator(s) and educates participants regarding study...DataTraineeshipWork at officeLocal areaShift work
$64.35k - $65k
...recruiting for the position of a Clinical Research Coordinator (CRC). The employee will... ...with study protocols, data documentation, reporting... ...related to human research participant protection and reports instances... ...protocol amendments, consent changes, and applicable protocol...DataTemporary workWork at officeLocal areaFlexible hours- Mount Sinai Morningside is seeking a Clinical Research Coordinator I to support daily activities of clinical studies, obtain informed consent, collect data, and assist with biospecimen... .../GCO processes. The role involves participation in NIH All of Us study activities,...Data
- ...Morningside is seeking an entry-level Clinical Research Coordinator to conduct and assist in clinical... ...role involves obtaining informed consent, collecting and organizing study... ...responsibilities such as data maintenance, participant screening, and assisting with site...Data
- ...Sinai Morningside is seeking a Clinical Research Coordinator to support human subjects research... .... You will obtain informed consent, collect and organize study data, and assist in grant submissions... ...documents. The role involves screening participants, maintaining confidential...Data
- ...please click here. Overview Clinical Research Coordinator I will oversee multiple... ...coordinator I will direct participants and study team members to... ...input, and preparing study data for presentation and submission... ...training. Screens and consents patients and ensures the...Data
$72.88k - $116.69k
...interprets highly complex clinical research data; conducts clinical testing... ...documents are submitted. Coordinates protocols and human subject... .... May obtain informed consent under general supervision... ...Investigator(s) and educate participants regarding study requirements...Data$16.5 - $38.48 per hour
Description The Clinical Research Coordinator, Part-time performs all the regular... ...studies, obtains informed consent, collects, maintains, and... ...Collects and records study data and inputs all information... ...investigator(s) and educates participants regarding study...DataHourly payPart timeTraineeshipWork at office- ...Philadelphia, PA 19107 The Clinical Research Coordinator I will work at site to... ...provide the best quality data to the sponsor. The CRC I... ...Clinical Investigators, Research Participants and Sponsor/CRO... ...concerns. Conduct patient consent discussions and ensure comprehension...Data
- Clinical Research Coordinator- McComb, MS ICON plc is a world-leading healthcare intelligence... ...studies, including participant recruitment, enrollment,... ...complete clinical trial data, including documentation of... ..., including informed consent forms, case report forms,...DataFlexible hours
$66.2k - $90k
Description A Clinical Research Coordinator (CRC) II position is currently available... ...activities such as data collection and management... ...required, obtain informed consent, collect, maintain and organize... ...answering phone calls, screening participants for eligibility,...DataTraineeshipWork at officeLocal area- SiteBridge Research Inc: Founded in 2021, SiteBridge... ...sponsored clinical research on time... ...Research Coordinator (Long Island, NY)... ...Communicate with study participants regarding study objectives... ...informed consent, and conducting protocol... ...and interpret data, taking note of...DataPart timeLocal area
$66.2k - $90k
...seeking a highly motivated Clinical Research Coordinator II (CRC II) to join our... ...operations, regulatory affairs, data management, patient‑facing... ...activities including participant outreach, scheduling, screening... ...criteria. Obtain informed consent under investigator...DataWork at office- ...across all diagnostic, treatment, and research services. The Clinical Research Coordinator (CRC) supports the conduct of clinical... ...coordinating trial operations including participant recruitment, informed consent, scheduling, data management, and regulatory documentation...DataWork at office
$54.69k - $82.04k
...$54,690.00 - $82,035.00 Clinical Research Coordinator Hemophilia Program Albany... ...Securing signed/completed consents and paperwork for eligible... ...to the patients/study. Participate in regional hemophilia... ...hemophilia research/data conferences, both virtually...DataFull timeLocal areaShift work$64.35k - $70k
Join to apply for the Clinical Research Coordinator - PACC role at Columbia University... ...Manage study participants by facilitating screening,... ...limited to recruiting and consenting patients, conducting study... ...source documentation and data entry. Collect, record, and...DataFull timeTemporary workWork at officeLocal area$70.48k - $88.24k
Position Summary Senior Clinical Research Coordinator (Senior CRC) at NYU Grossman... ...applicable regulations. Participate in sponsor meetings, feasibility... .... Obtain informed consent and assent for adult and pediatric... ...accurate and timely data entry in sponsor EDC systems...DataWork at officeRemote work- Description The Clinical Research Coordinator, Part-time performs all the regular... ...studies, obtains informed consent; collects, maintains and organizes... ...and records study data. Inputs all information into... ...(s) and educates participants regarding study requirements...DataHourly payPart timeTraineeshipWork at officeLocal area
- Description The Clinical Research Coordinator is an entry human subjects researcher... ...obtains informed consent, collects, maintains and organizes... ...older Chinese Americans. Participants will undergo a standard dementia... ...review of experimental data for publication and...DataHourly payTraineeshipWork at office
$70.48k - $74.79k
Position Summary The Oncology Clinical Research Coordinator (CRC) is an active participant in the coordination of oncology clinical... ...Research Coordinators (CRCs), Data Coordinator Unit (DCU) staff and... ...from pre-screening, through the consenting process, through the screening...DataWork at office$70.48k - $88.24k
...education, scientific research, and direct patient... ...team as a Senior Clinical Research Coordinator. The Senior Clinical... ...applicable regulations. Participate in sponsor meetings,... .... Obtain informed consent and assent for adult... ...accurate and timely data entry in sponsor EDC...DataWork at officeRemote work$58.66k - $73.53k
...Description The Clinical Research Coordinator I assists in the daily activities... ...studies, obtains informed consent; collects, maintains and organizes... ...and records study data. Inputs all information into... ...investigator(s) and educates participants regarding study...DataTraineeshipWork at officeLocal area- ...The Clinical Research Coordinator assists in the daily activities of clinical research... ...studies, obtains informed consent; collects, maintains and... ...and records study data. Inputs all information into... ...investigator(s) and educates participants regarding study requirements...DataFull timeTraineeshipWork at officeLocal area
- ...The Clinical Research Coordinator assists in the daily activities of clinical research... ...studies, obtains informed consent; collects, maintains and... ...Coordinator I will participate in clinical research activities... ...Collect and record study data and input all information...DataFull timeTraineeshipWork at officeLocal area
$17 - $41.08 per hour
...The Clinical Research Coordinator is an entry human subjects researcher, responsible... ...obtains informed consent, collects, maintains and organizes... ...consent, screening participants for eligibility, registering... ...and review of experimental data for publication and presentation...DataHourly payFull timeTraineeshipWork at officeLocal area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator I: Participant Consent & Data. Be the first to apply!
- clinical project manager remote New York, NY
- sr. clinical trial manager New York, NY
- global clinical trial manager New York, NY
- clinical research coordinator remote New York, NY
- senior clinical trials manager New York, NY
- clinical trials manager New York, NY
- clinical research coordinator ii New York, NY
- neuroscience clinical research coordinator New York, NY
- clinical project manager New York, NY
- remote clinical trial manager New York, NY


