Clinical Trials Coordinator

3 weeks ago


Étreux, Hauts-de-France, United States ClinLab Staffing Full time
Job Title: Protocol Associate I

At ClinLab Staffing, we are seeking a highly motivated and organized Protocol Associate I to join our team.

Key Responsibilities:

  • Oversee disease committees in all aspects of protocol development, including concept development, protocol development, NCI and CIRB submissions, quality control reviews, and tracking development timelines.
  • Assist with coordinating protocols for review, editing, and formatting for scientific and editorial accuracy.
  • Coordinate group-wide notification of study status changes, including activation, suspension, and termination.
  • Lead contact for disease chairs, investigators, and senior colleagues.
  • Maintain computer databases related to protocol development and status changes.
  • Plan and manage monthly teleconferences for assigned disease sites.
  • Generate committee tracking documents and prepare high-level notes from teleconferences.
  • Participate in departmental meetings, protocol development meetings, and conference calls.
  • Interact with other cooperative groups, the NCI, and member coordinators and investigators.
  • Prepare concept/LOI packets for submission to the ECOG-ACRIN Executive Committee.

Requirements:

  • Exemplary interpersonal, communication, and organizational skills.
  • Motivation, organization, and problem-solving skills.
  • Ability to manage multiple tasks and meet deadlines.
  • Ability to work as part of a team.
  • Bachelor's degree in a life science discipline or relevant professional experience.
  • Healthcare-related background and prior clinical and/or data services experience.

We offer a dynamic and supportive work environment with opportunities for growth and professional development.



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