Assistant Research Coordinator

Weill Cornell Medical CollegeNew York, NY
1d$29 - $37Onsite

About The Position

Under direction, assists with the coordination, implementation and management of all aspects of clinical research studies

Requirements

  • High School Diploma
  • Approximately 2-3 years of experience in an administrative support role, ideally in a clinical, academic or research setting.
  • Ability to take initiative and simultaneously manage multiple projects with minimal supervision.
  • Excellent communication skills (both verbal and written).
  • Demonstrated proficiency with MS Office Suite and database applications.

Nice To Haves

  • Bachelor's degree is preferred.

Responsibilities

  • Assists in the development of research designs.
  • Coordinates the recruitment and enrollment of study participants.
  • Assesses patient eligibility for inclusion in clinical trials.
  • Ensures proper consent protocols have been followed for study participation.
  • Advises study participants and families of trial activities and their rights as a study participant.
  • Performs monitoring of patients, collection and recording of clinical data.
  • Conducts patient follow up and arranges for diagnostic testing.
  • Analyzes research data using basic and advanced statistical methodologies; interprets results for clinical investigators and prepares reports.
  • Ensures strict adherence to study requirements according to guidelines set forth in the study protocol.
  • Coordinates specimen collection, transport, storage and processing.
  • Maintains ongoing records of trials for adverse events.
  • Provides sponsors with progress reports.
  • Compiles subject data collection and submission of case reporting forms to sponsoring company.
  • Produces summary data for each study and assists in the write up of completed projects.
  • Assists in database design programming and database management.
  • Coordinates and participates in site visits and audits. Ensures readiness and compliance. Addresses and resolves issues uncovered during visit/audit.
  • Assists with grant budgets and approvals.
  • Assists faculty in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.
  • Creates IRB and/or IACUC protocols, submits for review/approval and maintains correspondence with sponsoring agency, IRB and collaborative institutions.
  • Maintains research effort tracking for principle investigators and key personnel.
  • Performs other related duties as assigned.
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