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University at BuffaloPosted 16 days ago

Research Coordinator, Clinical Research Office

Full-time
On-site
Mid level
Competitive
Posted 16 days ago

Responsibilities Undertake coordinating tasks of clinical research studies Assist investigators in successful recruitment and retention of subjects Guide day-to-day operations of assigned studies, assuring adherence to protocol Generate accurate reports Resolve queries in a timely manner Maintain contact with Principal Investigator, monitoring agency, sponsor, and contracted vendors Generate IRB approved materials fo

Posted
16 days ago
Source
ubjobs.buffalo.edu
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Undertake coordinating tasks of clinical research studies
  • Assist investigators in successful recruitment and retention of subjects
  • Guide day-to-day operations of assigned studies, assuring adherence to protocol
  • Generate accurate reports
  • Resolve queries in a timely manner
  • Maintain contact with Principal Investigator, monitoring agency, sponsor, and contracted vendors
  • Generate IRB approved materials for distribution to study subjects to promote project enrollment and retention of enrolled subjects
  • Oversee implementation of research studies, generation of qualitative and quantitative data and data collection forms and surveys
  • Manage the day-to-day operations of the assigned project including development and implementation of research procedures and systems
  • Assist Principal Investigator with administration of clinical trial protocols, including obtaining informed consents and screening subjects, maintaining research records and research subject records, managing correspondence, researching medical records, recording data, and attending training sessions
  • Support the management of the CRO

Full job description

Responsibilities

  • Undertake coordinating tasks of clinical research studies
  • Assist investigators in successful recruitment and retention of subjects
  • Guide day-to-day operations of assigned studies, assuring adherence to protocol
  • Generate accurate reports
  • Resolve queries in a timely manner
  • Maintain contact with Principal Investigator, monitoring agency, sponsor, and contracted vendors
  • Generate IRB approved materials for distribution to study subjects to promote project enrollment and retention of enrolled subjects
  • Oversee implementation of research studies, generation of qualitative and quantitative data and data collection forms and surveys
  • Manage the day-to-day operations of the assigned project including development and implementation of research procedures and systems
  • Assist Principal Investigator with administration of clinical trial protocols, including obtaining informed consents and screening subjects, maintaining research records and research subject records, managing correspondence, researching medical records, recording data, and attending training sessions
  • Support the management of the CRO

Benefits

  • Being a part of the University at Buffalo community.
  • Research-intensive public university in New York.
  • Buffalo, New York, USA
  • http://www.buffalo.edu/
  • Late Stage
  • Total Funding
  • $22.95M
  • Key Investors
  • National Science Foundation
  • FuzeHub
  • 2023-01-09
  • Grant· $20M
  • 2022-08-06
  • Grant· $2.9M
  • 2022-04-13
  • Grant· $0.05M
  • Recent News
  • Bizjournals.com Feed (2025-11-12 15:43:17)
  • UB begins strategic plan process under new president
  • 2026-10-16
  • WNY's largest college saw employment grow nearly 10% over 5 years
  • 2026-10-03
  • News-Medical.Net
  • Blue LED lights help chemists build complex drug molecules
  • 2026-07-13
  • Company data provided by
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  • Customize Your Resume
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Required skills

Experience

  • Mid level

Job details

Employment type

Full-time

Seniority level

Mid level

Date posted

Oct 28, 2026

Work mode

On-site

Job source

ubjobs.buffalo.edu

Company

University at Buffalo

Healthcare

See all 7 jobs from University at Buffalo →
  • Buffalo, NY
  • Healthcare

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