Associate Director, Informed Consent Management

3 weeks ago


Princeton, New Jersey, United States Bristol-Myers Squibb Company Full time
Job Summary

The Associate Director, Informed Consent Management role is responsible for managing the end-to-end process for informed consent in BMS-sponsored clinical trials. This includes centralized triage, language modifications, and management of templates and processes.

The successful candidate will have a strong understanding of Good Clinical Practice (GCP) and Human Subject Research requirements, as well as experience in clinical operations and compliance.

This is a unique opportunity to join a dynamic team and contribute to the development of policies, procedures, and processes that ensure patient safety and quality.

Key Responsibilities
  • Manage the informed consent process for BMS-sponsored clinical trials
  • Develop and maintain policies, procedures, and processes for informed consent
  • Collaborate with cross-functional teams to ensure patient safety and quality
  • Provide subject matter expertise on informed consent processes
Requirements
  • Bachelor's degree in a scientific or technical discipline
  • At least 6-8 years of experience in the pharmaceutical industry
  • Strong understanding of GCP and Human Subject Research requirements
  • Experience in clinical operations and compliance


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