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Job detail

Clinical Research Coordinator

Northwell

Employer page
#FDA#Phlebotomy#Clinical Research#GCP#Patient Recruitment#Clinical Trials#IRB#Good Clinical Practice#Institutional Review Board
#Specimen Shipping
#Drug Accountability
#Grant Submission
Full TimeOn Site2-5 yrs$66,300 - $86,060 / YEARPosted 2 days ago

Location

New York

Salary

$66,300 - $86,060 / YEAR

Quick overview

Coordinates and monitors research trials, including the recruitment of participants and the collection and processing of biological specimens. Ensures adherence to good clinical practice, regulatory requirements, and study protocols while collaborating with investigators and the IRB.

Requirements summary

Requires a Bachelor's degree or equivalent experience with 1-3 years of relevant experience. Specifically seeks 2-3 years of experience as a Clinical Research Coordinator.

bachelor degreeRegulatory CompliancePhlebotomyData CollectionVenipunctureSpecimen ProcessingVital Signs MonitoringClinical Research CoordinationGood Clinical PracticeParticipant RecruitmentElectrocardiogramsDrug AccountabilityGrant Process Organization

Job description

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

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Northwell

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Hiring organization

Northwell

Northwell Health is New York State’s largest health care provider and private employer, with 28 hospitals, about 1,000+ outpatient facilities and more than 16,000 affiliated physicians. At Northwell, we focus on cultivating an environment that inspires growth, empowers...

Explore employer profile
IndustryHospitals and Health Care
TypeNonprofit
Size10,001+ employees
HQLake Success, NY
Founded1997
  • Bachelor's Degree required, or equivalent combination of education and related experience.
  • 1-3 years of relevant experience, required.
  • 2-3 years Clinical Research Coordinator experience
  • *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).

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