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Research Coordinator

WMCHealth

Suffern, NYPer Diem$35.29–44.37/hrSeen 3w agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$35.29–44.37/hr
Location
Suffern, NY
Schedule
Per Diem
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Research Coordinator administers and coordinates research study activities under the Operations Manager, supporting principal investigators, managing day‑to‑day operations, staffing, data collection, reporting, quality control, and adverse event documentation.

Skills & qualifications

RequiredNice to have

Skills

E‑Research TechnologyClinical TrialsData CollectionQuality ControlAdverse Event Reporting

Qualifications

Two to Three Years Experience in Academic Research or Pharmaceutical Industry SettingBachelor’s Degree in a Relevant Field

Full job description

Research Coordinator

Company: Good Samaritan Hospital

City/State: Suffern, NY

Category: Clerical/Administrative Support

Department: Cardiothoracic Surgeons Of GSH

Union: NO

Position: Per Diem

Shift: Per Diem

Req #: 13086

Posted Date: Sep 18, 2026

Hiring Range: $35.29 - $44.37

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External Applicant link Internal Applicant link

Job Details:

The Research Coordinator administers and coordinates research study associated activities under the direction of the Operations Manager and in coordination with the Principal Investigators (PIs).

Responsibilities:

  • Assists PIs with planning and coordinates the review and approval processes for research study protocols in accord with established policies and procedures.

  • Ensures the smooth and efficient day to day operations of research and data collection activities; acts as primary administrative point of contact for internal research staff (nurses, data manager, and pharmacist) and as the operational liaison for other research organizations, funding agencies and regulatory bodies.

  • Assists in training PIs and other research staff on the use of the e-research technology acquired by the NYRI.

  • Plans and coordinates staffing of research studies to include recruitment and administration of research support as appropriate to the initiative.

  • Supervises and coordinates the provision of support services to investigators and researchers

  • Monitors the progress of research activities; develops and maintains records of research activities and, with the PIs, prepares periodic and ad hoc reports as required by funding agencies and other regulatory bodies.

  • Implements quality control process throughout the conduct of trials.

  • Ensures that all serious and non-serious adverse events are properly documented and reported appropriately.

Qualifications/Requirements:

Experience: Two to three years of experience in academic research or pharmaceutical industry setting preferred, and previous experience with clinical trials, required.

Education: A Bachelor’s degree in a relevant field, required.

Licenses / Certifications: N/A

Other: N/A

Special Requirements: N/A

About Us:

Good Samaritan Hospital

Good Samaritan Hospital in Suffern, NY, is a 286-bed hospital providing emergency, medical, surgical, obstetrical/gynecological and acute-care services to residents of Rockland and southern Orange counties in New York; and northern Bergen County, NJ. The hospital is home to a recognized cardiovascular program, comprehensive cancer-treatment services, the area’s leading Wound and Hyperbaric Institute and outstanding maternal/child services that includes a Children’s Diagnostic Center. Good Samaritan Hospital also provides social, psychiatric and substance-abuse services and its certified home-care agency supports residents of the Hudson Valley and beyond.

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