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Medical External Funding Team Member

Clinical Trial
FDA
ICH
GCP
Description:

Basic Purpose

  • Support Medical Education, Research, and External Funding Team.
  • Ensure operational excellence across all grant and study processes while maintaining regulatory compliance and program oversight
  • Drive program improvement across all funding types (Medical Education, Sponsorships, External Research, and others).
  • Foster collaboration with external and internal partners.

 

Performance Indicators

  • Streamlined, compliant grants and funding process.
  • High satisfaction from internal and external partners.
  • Operational excellence and innovation at the center of execution.

 

Key Accountabilities

  • Oversee project management from intake to completion, including vetting requests and research proposals.
  • Provide insights and analytics to support project decision-making.
  • Address process and system barriers and coordinate logistics for local grants and research improvements.
  • Design and execution of key team/program annual projects.
  • Monitor budgets, ensuring responsible fund allocation.
  • Conduct training to enhance customer engagement.
  • Participate in review meetings to align grants and research with established protocols.

Skills & Abilities

  • Strong influence and collaboration skills.
  • Customer-centric mindset with proven experience in process improvement.
  • Creative problem-solving and executional urgency.
  • Excellent verbal communication and stakeholder engagement.
  • Familiarity with relevant regulations (FDA, ICH, IIS Best Practices, GxP (GCP/GDP), ACCME, OIG Guidelines).
  • Proficiency in:
    • Preparing meeting agendas, minutes, and presentations.
    • Developing tools and reports for grants and research.
    • Processing grants and research contracts.
    • Supporting clinical trial activities, including study milestones and compliance.
    • Managing clinical trial systems and drafting drug supply orders.
    • Understanding or willingness to learn medical education, external research, and pharmaceutical regulations.
    • Navigating workflows, databases, and systems supporting grants and research processes.

Bachelors Degree

QUALIFICATION/ LICENSURE :
  • Work Authorization : US Citizen
  • Preferred years of experience : 5+ Years
  • Travel Required : No travel required
  • Shift timings: Not specified
Job Location Ridgefield, Connecticut
Pay USD 55.00 - USD 69.00 Per Hour
Contract Duration 27 week(s)