Trabajos clinical research coordinator en New York, New York - Page 3Crear alertas

Description The Clinical Research Coordinator I assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.Assists in preparing grant applications and documents (for e.Institutional Review Board, Grants and Contracts Of

Assists in the activities related to clinical research including, but not limited to: obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering bilingual neuropsychological testing and questionnaires, and answering telephone call

Mount Sinai Health System is seeking a motivated Clinical Research Coordinator I (CRC I) to support an innovative ADHD research study focusing on treatment strategies for school-age youth. A Bachelor's or Master's degree in a scientific field is required, with research experience preferred.

A prestigious academic institution in New York seeks a Clinical Research Coordinator. This temporary role involves managing clinical trials, ensuring compliance, and collaborating with researchers. Familiarity with clinical research systems is preferred.

A clinical research organization in New Jersey is seeking a Registered Nurse for an Unblinded Clinical Research Coordinator role. Responsibilities include compounding and dispensing investigational products as part of clinical research trials, ensuring compliance, and maintaining medication records.

The Non‑therapeutic Oncology Clinical Research Coordinator (NT CRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout the conduct of clinical studies on various existing and upcoming protocols. Demonstrates competence in Good C

Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Responsibilities Conducts routine and standardized human

Position Summary The Clinical Research Coordinator provides research coordination support for multiple clinical research projects. Participation in the medical surveillance program: Contact with patients and/or human research subjects Successful completion of applicable compliance and systems trai

Mount Sinai Morningside is seeking an entry-level Clinical Research Coordinator in New York City.This role requires conducting human subjects research under supervision and maintaining study documentation.Candidates should hold a Bachelor's degree in science or a related field, along with 0-2 years

This is an hourly position which is eligible for overtime only intended to be used for part‑time employees. Job Description The Clinical Research Coordinator, Part‑time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption.

A clinical research organization in Jersey City, NJ, seeks a Clinic Research Coordinator II to ensure quality research at investigative sites following sponsor protocols.The ideal candidate will possess a high school diploma and a year of experience as a CRC, preferably in coordinating industry-spon

Preferred Qualifications Clinical Research Coordinator (CRC) Certification (preferred, required in some disciplines). Ensures accurate execution of research protocols in compliance with Good Clinical Practices, HIPAA and other obligations. Position Summary Responsible for providing moderate to adva

Description The Clinical Research Coordinator I assists in daily activities of clinical research studies, obtains informed consent, collects, maintains and organizes study information. The CRC I will, under minimal supervision, coordinate the implementation of a clinical research study with communit

A leading clinical research organization in Jersey City is seeking an Unblinded Clinical Research Coordinator II. The role involves compounding and dispensing Investigational Products for clinical trials, supervising medication records, and ensuring compliance with study protocols. Candidates must h

This is an hourly position which is eligible for overtime only intended to be used for part-time employees. Description The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours does not qualify for exemption. Mount

This is an hourly position which is eligible for overtime only intended to be used for part‑time employees. Job Description The Clinical Research Coordinator, Part‑time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption.

Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to assist in the daily activities of clinical research studies.

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.

Hackensack Meridian Health is seeking a Clinical Data Coordinator in Hackensack, NJ.The role includes data entry, managing queries for clinical research studies, and adhering to protocol requirements.Candidates should possess a BA/BS in a relevant field or equivalent experience.Strong organizational

NYU Langone Health is seeking a Research Coordinator for their Cardiac Cath Lab in New York. This role involves coordinating research studies, overseeing IRB submissions, and maintaining regulatory compliance.

Mount Sinai Medical Center is seeking a Clinical Research Coordinator I in New York, NY. In this role, you will assist in the daily activities of clinical research studies, coordinating efforts with community sites. Responsibilities include data collection, obtaining informed consent, and monitoring

Overview The Clinical Research Coordinator is an entry-level human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Responsibilities Conducts routine and standardized h

Job Description The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research Coordinator, but on an as‑needed basis. This individual assists in activities of clinical research studies, obtains informed consent; collects, maintains and organize

Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities related to clinical research studies including but not limited to: answering phone call

Columbia University is seeking a Clinical Research Coordinator to support investigator-initiated trials aimed at improving outcomes for patients with heart failure. The position offers a dynamic environment in clinical academic research. This role involves coordinating study activities, collecting d

Escalates issues of protocol non-compliance to study PI and research department leadership* Assess a protocol and study plan to develop a study budget. Clinical Research Coordinator page

American Oncology Network, LLC is seeking a Clinical Research Coordinator in Wayne, New Jersey. Candidates should possess previous oncology research experience, critical thinking skills, and proficiency with MS Office. The role involves managing clinical trials, ensuring protocol compliance, and mai

Overview The Clinical Research Coordinator is an entry-level human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Responsibilities Conducts routine and standardized h

A Brief Overview Working under the direction of the Institute for Clinical Research (ICR) and the Principal Investigator (PI), the Clinical Research Coordinator is responsible for end-to-end coordination and execution of clinical research studies conducted through the ICR. CCRC – Certified Clinica

Job Description The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities related to clinical research studies including but not limited to: answering phone

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. One year of research experience preferred Preferred Qualifications Prior experience in clinical research or healthcare Exp

The Non‑therapeutic Oncology Clinical Research Coordinator (NT CRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout the conduct of clinical studies on various existing and upcoming protocols. Competency in utilizing CRMS an

Mount Sinai Morningside in New York is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research studies. A Bachelor's or Master's degree in Science or a related field is required, with one year of research experience preferred.

A leading health system in New York is seeking a Clinical Research Coordinator to assist in daily clinical research activities. Join us in advancing healthcare through impactful research. No prior experience is required, though one year of research experience is preferred.

Complete and maintain the required training for participation in clinical research, including but not limited to Human Subjects Protection training and Clinical Research Coordinator Course. Outstanding technical writing skills and understanding of medical terminology and research. Coordinate day-to-

Clinical Research Coordinator The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Qualifications Bachelor’s degree in

Fort Wayne Medical Oncology & Hematology seeks a Clinical Research Coordinator to oversee clinical trials, manage patient care, and ensure regulatory compliance. The ideal candidate has a high school education, with a bachelor's preferred, and 2-5 years of oncology research experience.

Position: Unblinded Clinical Research Coordinator II Location: Jersey City, NJ Job Id: 1140 # of Openings: 1 Overview DM Clinical Research, the largest privately‑owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Cl

Overview Classification Title Clinical Research Associate I (Non-exempt) The Clinical Research Associate I (Clinical Research Coordinator) performs a vital role for the Division of Endocrinology, diabetes and Metabolism at the department of Medicine by coordinating various components of multiple cl

Job Title: Clinical Research Coordinator – Entry Human Subjects Researcher The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical researc

Mount Sinai Medical Center is seeking a Clinical Research Coordinator in New York, NY. This role involves conducting clinical research studies, obtaining informed consent, and collecting data. Candidates should possess a Bachelor's degree in science or a related field and have up to 2 years of resea

Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Responsibilities Conducts routine and standardized h

Overview The Clinical Research Coordinator is an entry-level human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. Responsibilities Conducts routine and standardized h

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening

Columbia University Irving Medical Center is seeking a Clinical Research Coordinator to support clinical trials through participant recruitment, data management, and compliance with safety standards.Ideal candidates possess a Bachelor's degree in clinical research, strong communication skills, and p

This role includes collecting and managing study data, obtaining informed consent from participants, and assisting with grant applications. Mount Sinai Health System seeks a part-time Clinical Research Coordinator in New York City.

Mount Sinai Health System in New York City is seeking a Clinical Research Coordinator to conduct and assist in clinical research studies under supervision. Candidates should have a bachelor's degree in science or a related field and 0-2 years of research experience.