Clinical Trial Project Coordinator

Baim Institute for Clinical Research

Boston (MA)

Presencial

USD 42.000 - 64.000

Jornada completa

Hace 9 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

The Baim Institute for Clinical Research in Boston seeks a Clinical Project Assistant, Safety Services to support CEC and DMC project teams. You will coordinate meetings, track trial metrics, manage study documents from start-up through closure, and assist the Senior Director of Safety Services while working in a fast-paced environment.

Responsibilities include preparing meeting materials, recording minutes, maintaining ISFs and subject diaries, coordinating investigator payments, and ensuring

Formación

  • Bachelor’s degree is required.
  • Clinical research experience preferred.
  • Strong organizational and communication skills.

Responsabilidades

  • Provide study related administrative assistance to CEC and DMC project teams.
  • Coordinate internal and external meetings, including agenda topics and minutes.
  • Manage tracking tools to support trial metrics for team leaders (Project Managers and team members).
  • Provide coordination and manage timelines for limited-service engagements.
  • Organize and maintain inventory of project supplies.
  • Coordinate printing and distribution of study materials (e.g., ISFs, subject diaries).
  • Coordinate investigator payment process.
  • Demonstrate ability to multi-task in a fast-paced environment.
  • Must be detail-oriented with strong prioritization and adaptability.
  • Proficiency in Word, Excel, PowerPoint, and Outlook; work independently and in a team.

Conocimientos

Meeting coordination
Document management
Multi-tasking
MS Office proficiency
Team collaboration

Educación

Bachelor's degree

Herramientas

Microsoft Word
Excel
PowerPoint
Outlook

Descripción del empleo

The Baim Institute for Clinical Research in Boston seeks a Clinical Project Assistant, Safety Services to support CEC and DMC project teams. You will coordinate meetings, track trial metrics, manage study documents from start-up through closure, and assist the Senior Director of Safety Services while working in a fast-paced environment.

Responsibilities include preparing meeting materials, recording minutes, maintaining ISFs and subject diaries, coordinating investigator payments, and ensuring

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