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Clinical Research Coordinator

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Northwell Health

Nov 12

Applications are closed

  • Job
    Full-time
    Junior & Mid Level
  • Research & Development
    Healthcare
  • New York

Requirements

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

Responsibilities

  • 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.

FAQs

What are the primary responsibilities of a Clinical Research Coordinator?

The primary responsibilities include coordinating research trials, overseeing participant recruitment, implementing study procedures, collecting and processing data, maintaining accurate records, and ensuring compliance with regulatory and grant agency requirements.

What qualifications are required for this position?

A Bachelor's Degree is required, or an equivalent combination of education and related experience, along with 1-3 years of relevant experience.

Is experience in clinical research necessary for this role?

Yes, 1-3 years of relevant experience in clinical research is required for this position.

Will I need to perform any medical procedures in this role?

Yes, the role may require performing venipuncture, ECGs, or monitoring vital signs on study participants as per study protocol.

Do I need certification to perform phlebotomy in this position?

While specific certification requirements may vary, phlebotomy training or certification is typically preferred or required for performing venipuncture.

Is collaboration with external agencies part of the job?

Yes, the Clinical Research Coordinator will liaise with external agencies, pharmaceutical companies, laboratories, and equipment and supply companies as necessary.

What does "good clinical practice" mean in this context?

Good clinical practice refers to the ethical and scientific quality standards for designing, conducting, recording, and reporting trials that involve human subjects, ensuring their safety and dignity throughout the research process.

Are there opportunities for advancement in this position?

Yes, there can be opportunities for advancement based on performance, experience, and further education within the field of clinical research.

What kind of work environment can I expect in this role?

The work environment may vary, often involving collaboration with healthcare professionals, researchers, and study participants, and may include both office-based and clinical settings.

How is salary determined for this position?

The salary is determined based on several factors including location, specialty, years of relevant experience, education, credentials, and budget considerations, and may be modified in the future.

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Northwell Health

We’ve re-imagined what health care can be. Are you Made for this?

Science & Healthcare
Industry
10,001+
Employees
1997
Founded Year

Mission & Purpose

Northwell Health is New York State’s largest health care provider and private employer, with 21 hospitals, about 900 outpatient facilities and more than 12,000 affiliated physicians. We care for over two million people annually in the New York metro area and beyond, thanks to philanthropic support from our communities. Our 85,000 employees – 18,900 nurses and 4,900 employed doctors, including members of Northwell Health Physician Partners – are working to change health care for the better. We’re making breakthroughs in medicine at the Feinstein Institutes for Medical Research. We're training the next generation of medical professionals at the visionary Donald and Barbara Zucker School of Medicine at Hofstra/Northwell and the Hofstra Northwell School of Nursing and Physician Assistant Studies

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