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Senior Research Coordinator

1 month ago

New York, New York, United States NYU Langone Medical Center Full time
Job Description

NYU Grossman School of Medicine is one of the nation's top-ranked medical schools, with a rich history of training physicians and scientists who have made significant contributions to the field of medicine.

The Senior Research Coordinator will play a critical role in managing day-to-day study operations and participant activities across two research studies. This includes developing study-specific project plans, managing timelines, resources, and project milestones, as well as providing day-to-day project management for research as assigned.

The ideal candidate will have a strong understanding of clinical research coordination and management, with experience in managing research studies, including protocol compliance, staff supervision, participant management, data quality, problem resolution, and leadership and coordination of the study team.

The Senior Research Coordinator will also be responsible for communicating with the Principal Investigator (PI) regarding study operations and achievement of study goals, as well as providing weekly progress reports to the PI and research team.

This is an exciting opportunity to join our team and contribute to the advancement of medical research.

Key Responsibilities
  • Develop study-specific project plans and SOPs, from study initiation through recruitment close out and final reporting
  • Manage timelines, resources, and project milestones in conjunction with PI, project team, and sponsor
  • Provide day-to-day project management for research as assigned, including protocol compliance, staff supervision, participant management, data quality, problem resolution, and leadership and coordination of the study team
  • Communicate with PI regarding study operations and achievement of study goals
  • Provide weekly progress reports to PI and research team
Requirements
  • Bachelor's degree or equivalent in business administration, health care administration, or related discipline
  • Minimum of four years of progressively responsible related experience coordinating clinical/research trials studies
  • Proficiency in using various Microsoft Office applications, including Word, Excel, Access, PowerPoint, and Outlook
  • Familiarity with Internet applications
  • Effective oral, written, communication, and interpersonal skills
  • Ability to interface effectively with all levels of management and work and communicate effectively with both internal and external customers
  • Ability to work within a team environment as well as independently
  • Ability to work and make decisions independently
  • Time management skills and ability to multi-task
  • Strong understanding and knowledge base of coordination requirements associated with clinical/research trials
  • Ability to identify, analyze, and solve problems; ability to work well under pressure