Clinical Research Project Coordinator

University at Buffalo

Amherst (MA)

Presencial

USD 60.000 - 90.000

Jornada completa

Hace 9 días

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Descripción de la vacante

The University at Buffalo's Clinical Research Office is seeking a Research Coordinator to support multiple clinical studies, coordinate recruitment and retention, and oversee day-to-day study operations. The role reports to the CRO Associate Directors and involves ensuring protocol adherence and data collection across studies.

Minimum qualifications include a Bachelor's degree and 2 years of clinical research experience, with familiarity with clinical research procedures.

Formación

  • Bachelor's degree and 2 years of clinical research-related experience or an equivalent combination of education and experience.
  • Applicants must be familiar with clinical research procedures and methodology.

Responsabilidades

  • Coordinate tasks of clinical research studies.
  • Assist investigators in recruitment and retention of subjects.
  • Guide day-to-day operations of assigned studies, ensuring adherence to protocol.
  • Generate accurate reports.
  • Resolve queries in a timely manner.
  • Maintain contact with Principal Investigator, monitoring agency, sponsor, and vendors.
  • Generate IRB-approved materials for distribution to study subjects.
  • Oversee implementation of studies and data collection forms/surveys.
  • Manage day-to-day operations including development and implementation of procedures and systems.
  • Assist PI with administration of clinical trial protocols, including informed consents and subject screening.

Conocimientos

Clinical research procedures

Educación

Bachelor's degree
2 years experience in clinical research

Descripción del empleo

The University at Buffalo's Clinical Research Office is seeking a Research Coordinator to support multiple clinical studies, coordinate recruitment and retention, and oversee day-to-day study operations. The role reports to the CRO Associate Directors and involves ensuring protocol adherence and data collection across studies.

Minimum qualifications include a Bachelor's degree and 2 years of clinical research experience, with familiarity with clinical research procedures.

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