Research Coordinator
$35.29 - $44.37 per hourWMCHealth
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
Apply Now
External Applicant link Internal Applicant link
*If you are hired by WMCHealth, your final base salary will be determined based on job-related factors, including employment status (full-time, part-time or per diem), relevant skills, qualifications and experience. Consistent with our commitment to pay equity, we also consider internal equity among similarly situated employees when determining final compensation.
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.
Apply Now
External Applicant link Internal Applicant link
Talent Community
Search Jobs
Hiring Events (- ...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...Suggested
$70k - $80k
...Research Coordinator Circuit Clinical® is on a mission to transform how people find, choose, and participate in clinical research. We are challenging the historical clinical trial methodologies through our work focused on improving access and inclusion in community...SuggestedFull timeContract workPart timeWork at officeRemote work- ...functional project leader responsible for delivering clinical research business initiatives through effective project execution, stakeholder... ...and optimization of clinical research technology platforms, coordinating requirements gathering, testing, deployment, and adoption...SuggestedFull timeFor contractors
$29.34 - $36.67 per hour
...Position Summary Coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research; acts as the patient...SuggestedHourly payFull timeTemporary workPart timeLocal areaFlexible hoursShift work- ...Replacement division. This hybrid role based in Mahwah, NJ, combines strategic project leadership with hands‑on execution to advance research initiatives, optimize workflows, and ensure regulatory readiness throughout the project lifecycle. You will develop plans, manage...Suggested
- ...what skills, including and relevant soft skills and software package proficiencies, are required. The Clinical Research Revenue Cycle Coordinator is responsible for ensuring accurate and compliant billing for clinical trials, collaborating with revenue cycle teams...Work at officeShift work
$70k - $90k
We are a leading world supplier of integrated processing solutions for customers in the area of pharmaceuticals, food processing, feeds and fine chemicals. Our products and services stand for reliability and quality worldwide. About 3,000 employees work for Glatt at more...Work at officeWorldwide- ...Director or above CDP Development and Management: • Supports the planning, execution and reporting of clinical programs/ trials Clinical Research Protocols • Reviews Clinical Protocols Study Management • Reviews study documents (i.e., investigator databases, ICFs, IEC/ IRBs...For contractorsImmediate start
- ...Health, and Specialty Products.POSITION SUMMARY:The Director of Research & Development Portfolio Management serves as the R&D leader... ...Director leads a team of project managers and provides structure and coordination across Food Solutions, Minerals & Nutrients, and Technical...Worldwide
- ...Fair360 and others. If you're as passionate about your future as we are, join our team.KPMG is currently seeking a Director, Tax Research and Planning to join our Firm Tax team.Responsibilities:Lead and oversee tax research and analysis related to the preparation of individual...H1bLocal area
$110.2k - $176.4k
...compliance with Good Clinical Practices, and all National and Local Regulations. Responsibilities: Develops and authors clinical research protocols, ensuring alignment with study objectives, regulatory requirements, and scientific standards. Manages essential study...Daily paidTemporary workWork at officeLocal areaRemote workFlexible hoursShift work$210k - $245k
...NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We're exploring the potential of cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan. Summary : Accountable for the oversight, management,...Temporary workWork at officeFlexible hours$120k - $130k
...NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We're exploring the potential of... ..., and closing clinical studies. Must be able to manage and coordinate with the Clinical Lead(s), Study Manager(s), Operations Program...Temporary workWork at officeLocal areaFlexible hours$83.78k
...keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change. The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in...Hourly payFull timePart timeApprenticeshipWork experience placementWork at officeLocal areaShift workNight shiftWeekend workAfternoon shift- ...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Clinical Research Coordinator Full Time Ridgewood, NJ, US Summary: The Clinical Research Coordinator will manage the day-to-day operations of...Full timeTemporary workWork at officeLocal areaFlexible hours
- PDI is seeking a Laboratory Associate for 1st shift (Mon-Fri, 6:00am - 2:30pm) in New York. Responsibilities include validating incoming raw materials against USP/SOPs, performing chemical testing, and maintaining precise documentation in the analytical lab. The role requires...Day shift
- PDI is seeking a Laboratory Associate for 1st shift in New York to perform chemical testing on incoming raw materials according to USP, SOPs, and NPTM. You will document results, assist in sampling and release, and maintain lab records in LIMS with attention to accuracy...Work at officeDay shift
$35 - $41.43 per hour
Job Description Job Description Job Title: Analytical Chemist III Location: Pearl River, NY Type: Contract Compensation: $35-$41.43 Work Model: Onsite – onsite Hours: 40.0 Overview Leading pharmaceutical company looking for an experienced Analytical...Contract workLocal area- ...send your CV and application through as soon as possible. A Research Leadership Opportunity for an NP or PA Are you a Nurse... ...investigator CVs, financial disclosures, delegation records, and coordination of radiation dosimetry documentation and required approvals....Contract workImmediate start
$27 - $33.14 per hour
Job Description Job Description Job Title: Analytical Chemist II Location: Pearl River, NY Type: Contract Compensation: $27-$33.14 Work Model: Onsite – onsite Hours: 40.0 Overview Leading pharmaceutical company looking for an experienced Analytical...Contract workLocal area- Job Description Job Description Position Summary Rotatek is seeking an experienced Vibration & Balancing Engineer to join our growing field engineering team. The successful candidate will perform vibration diagnostics, field balancing, machinery troubleshooting,...Daily paidWork at office
- ...standards. Responsibilities Develop and author clinical research protocols aligned with study objectives and regulatory requirements... ...and laboratories Lead budget and timeline development, coordinate site selection and training, ensure efficient execution...
- ...this career opportunity and how it fits into our organizations success. Summary of the Job: In this role you will lead research coverage on a specific industry sector delivering insightful investment research to institutional clients. You will be responsible...Full timeTemporary workWork at office
- ...Role is Exciting At Behaviorally, you'll do more than manage research—you'll help shape the future of how global brands understand... ...professional development and ensuring the highest quality standards. Coordinate with internal teams and external vendors to keep initiatives...Work at office3 days per week
- PDI, a leader in healthcare products, is seeking a 3rd shift Analytical Chemist (Sun-Thu, 11:00 PM-7:30 AM) to analyze incoming raw materials per USP, SOPs, and GMPs, ensuring only compliant materials are released and documenting results. You will perform pH, viscosity,...Night shift
- Summit Clinical Research Solutions is seeking a Clinical Research Coordinator to manage day‑to‑day trial operations, recruit and screen participants, and ensure protocol and regulatory compliance. The role requires strong communication, multi‑tasking, and collaboration...
- NS Pharma in Paramus, NJ is seeking a Manager, Clinical Research to execute global clinical studies with adherence to FDA, ICH, local regulatory requirements and NS Pharma SOPs. This hybrid role requires travel to the Paramus office at least twice a week and involves planning...Work at officeLocal area
- Hackensack Meridian Health is seeking a Clinical Research Coordinator to coordinate and oversee clinical operations for assigned trials, ensuring compliant conduct under PI supervision. The role demands meticulous attention to regulatory polices, SOPs, and quality assurance...Work at office
- NS Pharma Inc., Paramus, NJ, is hiring a Manager, Clinical Research to support global clinical studies in a hybrid role. The position requires coordinating study activities, overseeing vendors, and ensuring regulatory compliance. The role emphasizes collaboration with...
- Summit Clinical Research Solutions is seeking a Clinical Research Coordinator in Ridgewood, NJ to manage day-to-day trial operations and ensure protocol and regulatory compliance. You will recruit and screen participants, document activities, and report on study progress...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Research Coordinator. Be the first to apply!





