Clinical Research Coordinator

Northwell Health
Staten Island, NY, United States
Full-time

Job Description

  • Coordinates and monitors research trials; actively oversees the recruitment of study participants. May be required to perform venipuncture on study participants;
  • collects, processes, and ships specimens according to protocol and training requirements. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol;

maintains study records and collaborates with the institutional review board as necessary.

Job Responsibility

  • Responsible for coordination of a designated study or group of studies.
  • In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data.
  • Keeps accurate and up-to-date records.
  • Collects labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements.
  • Schedules subjects for protocol-related evaluations; collaborates with physicians, investigators and other healthcare providers;

promotes respect for subjects' rights.

  • Administers, scores and evaluates results of assessments as assigned and as related to study protocol; collects data, confers with PI and forwards results to sponsor (internal or external).
  • Interfaces with external agencies as necessary; organizes all phases of grant process for submission to funding agencies as necessary.
  • Ensures availability of drug supplies and / or equipment for studies; maintains drug accountability logs.
  • Liaisons with agencies and pharmaceutical companies, laboratories, and equipment and supply companies, as needed.
  • Adheres to good clinical practice, and complies with regulatory and grant agency requirements; follows protocol as developed and keeps investigator or supervisor informed of developments.
  • Collaborates with PI and the food and drug administration and drug companies on related issues; may be required to perform phlebotomy, electrocardiograms, or monitor vital signs on study participants and report findings to supervisor.
  • Operates under general guidance and work assignments are varied and require interpretation and independent decisions on course of action.
  • Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act.

Duties not mentioned here, but considered related are not essential functions.

Job Qualification

  • Bachelor's Degree required, or equivalent combination of education and related experience.
  • 1-3 years of relevant experience, required.
  • Additional Salary Detail

The salary range and / or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future.

When determining a team member's base salary and / or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

8 days ago
Related jobs
Promoted
Columbia University
New York, New York

We are seeking a clinical research coordinator (CRC) for the ALS Center at Columbia University Medical Center. Irving Clinical Research Center, Research Pharmacy, local laboratories, radiology). Coordinates and conducts in-person and remote study visits by communicating closely with patients, hospit...

Promoted
Northwell Health
New York, New York

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as necess...

Promoted
Columbia University
New York, New York

The Columbia Center for Translational Immunology (CCTI) at Columbia University Irving Medical Center (CUIMC) is actively seeking a dynamic and proficient Clinical Research Coordinator to bolster our research endeavors. Participate in clinical transplant meetings, collaborating with clinical and rese...

Promoted
Medix™
New York, New York

Clinical Research (Fundamental Awareness): Knows the primary resources available to accomplish the job. Can successfully research simple clinical questions pertaining to the functional area. Participates in periodic site visits from sponsor, regulatory authorities and others to review research, sour...

Northwell Health
Staten Island, New York

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as necess...

Actalent
New York, New York

Study Coordinator or Clinical Research Coordinator role. This is a contract position and requires previous Oncology clinical research experience*. ...

NYU Langone Health
New York, New York

The Clinical Research Coordinator is an active participant in the coordination of critical care and resuscitation research studies from research planning to completion of studies. The Clinical Research Coordinator performs study coordination tasks under the direction of the investigator and works cl...

DM Clinical Research
Brooklyn, New York

Clinic Research Coordinator II   The  Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. ...

NYU Langone
New York, US

We are seeking a highly organized and dedicated Clinical Research Coordinator to join our research team in the Division of Laryngology. We have an exciting opportunity to join our team as a Clinical Research Coordinator. Help to reconcile any clinical discrepancies in data with RDAs and RCs; assist ...

NYU Langone
New York, US

The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) 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. Maintains basic knowledg...