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Weill Cornell MedicinePosted 25 days ago

Research Coordinator

Full-time
On-site
2+ years
$68K – $78K/yr
Posted 25 days ago

Weill Cornell Medicine seeks a Research Coordinator to oversee data management, regulatory, and financial aspects of clinical trial operations. The role also coordinates research projects, supports protocol development, and manages recruitment strategies and study budgets.

Posted
25 days ago
Source
jobs.weill.cornell.edu
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Develops and implements practices to ensure research efficiency by routinely analyzing and evaluating workflow
  • Coordinates the collection, compilation, documentation and analysis of clinical research data from various clinical sites. Assists in the determination of guidelines for the collection of clinical data and or administration of clinical studies
  • Ensures compliance of general and study specific regulatory related processes with SOPs, FDA, NIH, and applicable regulations for the reporting of events to regulatory agencies
  • Develops regulatory reports and associated documentation in accordance with SOPs and study specific processes
  • Prepares study related budgets for granting agencies. Negotiates study related budgets with various sites, departments and sponsors
  • Researches and develops the recruitment strategies. Employs modeling and simulation tools to understand the current and projected outcome of recruitment techniques. Monitors and evaluates the success of varying subject recruitment techniques
  • Participates in protocol development as it relates to patient recruitment. Assesses, analyzes, prepares and submits departmental protocols to various places as it relates to subject recruitment and retention
  • Performs monitoring visits: pre-study, initiation, routine monitoring and closeout visits
  • Works closely with sponsor, site and study personnel on relevant regulatory issues. Develops policies and procedures pertaining to regulatory and monitoring processes. Leads regulatory educational training events for personnel at various sites
  • Maintains inventory of supplies, equipment and/or reagents. May order supplies/equipment/reagents as authorized or ensure that needs are escalated appropriately. Receives supply orders and confirms accuracy of delivery. May assist with cost control
  • Performs other related duties as directed

Qualifications

  • Bachelor's Degree in related field
  • Approximately 2 years of experience in health-related role, in clinical or research setting
  • Experience with conducting and carrying out protocols and research coordination
  • Familiarity with IRB interaction, regulatory policies, database input and report generation
  • Research experience in an academic health center with exposure to a team research environment at all levels (senior investigators, nurses, research coordinators, lab technicians)
  • 3.8
  • Weill Cornell Medicine is an academic medical institution that offers health care services.
  • New York, New York, USA
  • https://careers.weill.cornell.edu
  • Distribution of Different Job Fields Receiving Sponsorship
  • Represents job field similar to this job
  • Engineering and Development
  • Education and Training
  • Customer Service and Support
  • Management and Executive
  • Legal and Compliance
  • Accounting and Finance
  • Trends of Total Sponsorships
  • (146)
  • (171)
  • (201)
  • (198)
  • (151)
  • (125)
  • $74.8M

Required skills

Clinical ResearchIRB ProcessesRegulatory ComplianceResearch CoordinationResearch Protocols

Full job description

Weill Cornell Medicine seeks a Research Coordinator to oversee data management, regulatory, and financial aspects of clinical trial operations. The role also coordinates research projects, supports protocol development, and manages recruitment strategies and study budgets.

Responsibilities

  • Develops and implements practices to ensure research efficiency by routinely analyzing and evaluating workflow
  • Coordinates the collection, compilation, documentation and analysis of clinical research data from various clinical sites. Assists in the determination of guidelines for the collection of clinical data and or administration of clinical studies
  • Ensures compliance of general and study specific regulatory related processes with SOPs, FDA, NIH, and applicable regulations for the reporting of events to regulatory agencies
  • Develops regulatory reports and associated documentation in accordance with SOPs and study specific processes
  • Prepares study related budgets for granting agencies. Negotiates study related budgets with various sites, departments and sponsors
  • Researches and develops the recruitment strategies. Employs modeling and simulation tools to understand the current and projected outcome of recruitment techniques. Monitors and evaluates the success of varying subject recruitment techniques
  • Participates in protocol development as it relates to patient recruitment. Assesses, analyzes, prepares and submits departmental protocols to various places as it relates to subject recruitment and retention
  • Performs monitoring visits: pre-study, initiation, routine monitoring and closeout visits
  • Works closely with sponsor, site and study personnel on relevant regulatory issues. Develops policies and procedures pertaining to regulatory and monitoring processes. Leads regulatory educational training events for personnel at various sites
  • Maintains inventory of supplies, equipment and/or reagents. May order supplies/equipment/reagents as authorized or ensure that needs are escalated appropriately. Receives supply orders and confirms accuracy of delivery. May assist with cost control
  • Performs other related duties as directed

Company

  • Academic medical institution providing patient care, research, and physician education
  • New York, New York, USA
  • https://careers.weill.cornell.edu/
  • Founded in 1898
  • 5001-10000 employees

Qualifications

  • Bachelor's Degree in related field
  • Approximately 2 years of experience in health-related role, in clinical or research setting
  • Experience with conducting and carrying out protocols and research coordination
  • Familiarity with IRB interaction, regulatory policies, database input and report generation
  • Research experience in an academic health center with exposure to a team research environment at all levels (senior investigators, nurses, research coordinators, lab technicians)
  • Glassdoor
  • 3.8
  • Weill Cornell Medicine is an academic medical institution that offers health care services.
  • New York, New York, USA
  • https://careers.weill.cornell.edu
  • H1B Sponsorship
  • Data Powered by
  • Distribution of Different Job Fields Receiving Sponsorship
  • Represents job field similar to this job
  • Engineering and Development
  • Education and Training
  • Customer Service and Support
  • Management and Executive
  • Legal and Compliance
  • Accounting and Finance
  • Marketing
  • Trends of Total Sponsorships
  • *2026
  • (146)
  • 2025
  • (171)
  • 2024
  • (201)
  • 2023
  • (198)
  • 2022
  • (151)
  • 2021
  • 2020
  • (125)
  • Late Stage
  • Total Funding
  • $74.8M
  • Key Investors

Required skills

  • Clinical Research, IRB Processes, Regulatory Compliance, Research Coordination, Research Protocols

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 19, 2026

Work mode

On-site

Job source

jobs.weill.cornell.edu

Company

Weill Cornell Medicine

Healthcare

Academic medical institution providing patient care, research, and physician education

See all 14 jobs from Weill Cornell Medicine →

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Research Coordinator

Weill Cornell Medicine · $68K – $78K/yr

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