Research Manager Leader

5 days ago

Bengaluru, Karnataka, India beBeeDirector Full time ₹ 1,50,00,000 - ₹ 2,00,00,000

Job Summary:

The Senior Clinical Research Director oversees clinical trials and research studies, ensuring timely completion and compliance with regulatory standards.

About the Role:

  • Clinical Trial Management:
    • Plan, initiate, and manage research projects from start to finish.
    • Coordinate and oversee the execution of clinical trials, ensuring adherence to protocols, timelines, and budgets.
    • Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and ethical standards.
  • Team Leadership:
    • Lead and mentor research staff, ensuring they are trained and performing effectively.
    • Assign tasks and responsibilities to team members based on project needs.
    • Develop training programs and provide ongoing professional development for research teams.
  • Regulatory Compliance:
    • Oversee the preparation and submission of regulatory documentation, including Institutional Review Board (IRB) applications and clinical trial applications.
    • Monitor compliance with federal, state, and local regulations, as well as company policies.
    • Ensure timely reporting of adverse events and ensure the study meets ethical and regulatory standards.
  • Study Design & Protocol Development:
    • Work with scientific and medical teams to develop clinical trial protocols.
    • Ensure protocols meet study objectives, regulatory standards, and ethical guidelines.
    • Evaluate feasibility and risk of proposed studies.
  • Data Management and Reporting:
    • Ensure data collection, monitoring, and analysis are conducted efficiently and accurately.
    • Review and analyze clinical trial data to ensure quality and integrity.
    • Prepare and present progress reports to senior leadership and stakeholders.
  • Budget and Resource Management:
    • Develop and manage project budgets, ensuring that clinical trials are completed within financial constraints.
    • Oversee resource allocation, including personnel, equipment, and materials.
  • Collaboration and Communication:
    • Foster communication between internal teams, external partners, and key stakeholders.
    • Collaborate with research coordinators, data managers, and other departments to ensure effective study execution.
    • Resolve any issues related to clinical trial execution and provide solutions.
  • Continuous Improvement:
    • Identify areas for process improvement in clinical trial execution and management.
    • Implement best practices to optimize research efficiency and compliance.

Requirements:

  • Bachelor's degree in Life Sciences, Clinical Research, or a related field (Master's or higher preferred).
  • 8-18 years of Experience in clinical research, with at least 2-3 years in a managerial or supervisory role.
  • In-depth knowledge of clinical trial management, regulatory requirements, and GCP.

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