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Medical and Regulatory Affairs Specialist

1 month ago

Jersey City, New Jersey, United States Omni Inclusive Full time
Job Summary

We are seeking a highly skilled Medical and Regulatory Affairs professional to join our team at Omni Inclusive. The successful candidate will be responsible for managing daily operations of MI vendors, navigating matrix partnerships, and ensuring accurate resources are available to execute on stakeholder needs.

Key Responsibilities
  • Manage daily operations of MI vendors, including oversight on escalations, standard response document maintenance, and variant process in conjunction with Associate Director.
  • Navigate matrix partnerships to ensure operational excellence and strategic decision making.
  • Ensure accurate, balanced, and current resources are available and communicated to execute on stakeholder needs, content deliverables compliantly and with a high level of quality.
  • Work with business solutions partners to optimize use of system and technology.
  • Identify continuous improvement opportunities in alignment with the Customer Engagement Center strategic objectives.
  • Engage, participate, and drive initiatives of the External Engagement and Enablement organization.
Essential Requirements
  • PharmD degree.
  • Experience in the pharmaceutical or related industry, including MI, and ability to demonstrate knowledge of MI function.
  • Broad understanding of diseases and pharmacotherapy, with specific disease state and pharmacotherapy knowledge in Immuno-Oncology, CV, or Immunoscience.
  • Working knowledge of Medical Information and content creation, including ability to evaluate information from multiple sources.
What We Offer

At Omni Inclusive, we offer a dynamic and supportive work environment, with opportunities for professional growth and development. If you are a motivated and detail-oriented individual with a passion for Medical and Regulatory Affairs, we encourage you to apply for this exciting opportunity.