Actalent - Boston, MA

posted 9 days ago

Full-time - Mid Level
Remote - Boston, MA
10,001+ employees
Administrative and Support Services

About the position

As a Clinical Study Manager, you will be responsible for the planning and execution of clinical studies, focusing on developing integrated study plans and overseeing site selection and qualification. This role involves acting as a project manager for the clinical study team, ensuring compliance with quality measures, managing budgets, and providing oversight for CRO-generated documents. You will also support knowledge management and departmental training efforts within a collaborative work environment.

Responsibilities

  • Develop a cross-functional, integrated study plan for clinical studies.
  • Oversee site selection and qualification processes.
  • Act as a project manager for the clinical study team, coordinating with internal stakeholders and CROs.
  • Ensure operational delivery aspects of the protocol are met.
  • Manage study budgets and ensure compliance with quality measures.
  • Provide oversight for CRO-generated documents.
  • Support knowledge management and departmental training efforts.

Requirements

  • Experience in global clinical trial management.
  • Background in oncology and Phase III clinical trials.
  • Strong vendor management skills.
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