Senior Manager, Medical Research

in Healthcare + Life Sciences Contract

Job Detail

  • Experience Level Sr Level
  • Degree Type Bachelor of Science (BS)
  • Employment Contract
  • Working Type Hybrid
  • Job Reference 0000015385
  • Salary Type Hourly
  • Industry Pharmaceuticals
  • Selling Points

    Lead impactful research initiatives in a dynamic, global environment. Collaborate with cross-functional teams to ensure high-quality study execution. Hybrid work arrangement offering flexibility and engagement.

Job Description

Overview

  • Lead operational execution and oversight of Investigator Initiated Studies and Research Collaborations in a dynamic, global environment.
  • Serve as a central contact for investigators, internal teams, and vendors, ensuring high-quality research execution.
  • Coordinate study lifecycle activities, including concept intake, review, contracting, execution, and close-out.
  • Collaborate with cross-functional teams to maintain inspection readiness and support audits and inspections.
  • Manage IIS and RC budgets, ensuring compliance with local/regional requirements and quality standards.
  • Contribute to initiatives aimed at improving investigator experience and internal efficiencies.
  • Uphold and model core values in all aspects of work, fostering a collaborative environment.
  • Hybrid work arrangement offering flexibility and engagement with global teams.

Key Responsibilities & Duties

  • Act as the primary contact for IIS and RC activities across multiple regions.
  • Manage relationships with investigators, academic partners, and internal stakeholders.
  • Coordinate Medical Affairs Review Board meetings, including agenda development and document preparation.
  • Track IIS/RC metrics and provide updates to Medical Affairs leadership.
  • Collaborate with GPSRM and QA teams to support audits and inspections.
  • Ensure compliance with drug shipment activities and quality standards.
  • Identify operational challenges and propose practical solutions to improve processes.
  • Provide oversight for IIS portal vendor issues and updates.

Job Requirements

  • Bachelor’s degree in Life Sciences or related field; advanced degree preferred.
  • Minimum of 5 years of experience in pharmaceutical/biotech industry; 7 years preferred.
  • Proven expertise in Clinical Operations and Medical Affairs supporting GCP/GPP studies.
  • Strong knowledge of ICH/GCP, regulatory guidelines, and clinical research processes.
  • Excellent communication skills and stakeholder management capabilities.
  • Highly organized, detail-oriented, and able to work independently.
  • Solution-oriented mindset with strong problem-solving skills.
  • Hybrid work arrangement requiring adaptability and collaboration with global teams.
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