Remote Otter LogoRemoteOtter

Senior Central Risk Manager - Remote

Posted 41 weeks ago
All others
Full Time
India

Overview

The Senior Central Risk Manager plays a pivotal role in developing and executing risk-based monitoring strategies, ensuring data quality and integrity in clinical research projects. This position involves cross-functional collaboration to identify, assess, and mitigate risks throughout the clinical trial lifecycle, supporting the seamless implementation of Risk-Based Study Management (RBSM) principles.

In Short

  • Provide subject matter expertise for developing and updating the risk-based monitoring strategy tailored to project needs.
  • Collaborate with cross-functional teams to identify and mitigate risks associated with complex indications.
  • Draft initial risk assessments and support the finalization of Risk Assessment and Categorization Tools (RACT).
  • Guide Project Managers (PMs) in transferring identified risks to the appropriate tracking systems and ensure ongoing reviews.
  • Advise on developing functional plans to mitigate risks effectively.
  • Utilize available tools to conduct remote data reviews and centralized statistical monitoring, identifying risks to data quality and integrity.
  • Facilitate internal and sponsor reviews of findings, seeking cross-functional support for complex risks and mitigations.
  • Deliver initial and ongoing training for study teams on risk assessment, centralized monitoring, and risk-based monitoring strategies.
  • Mentor peers and train new team members on functional delivery, risk evaluation, and action implementation.
  • Escalate risks or deliverables at risk to the PM, including scope changes.

Requirements

  • Bachelor’s degree in a field relevant to clinical research; Master’s degree or health data sciences degree preferred.
  • Expertise in Good Clinical Practice/ICH E6 (R3) Guidelines and other regulatory requirements.
  • Proficiency in Risk-Based Monitoring strategies, processes, and tools.
  • Minimum of 5 years in risk management within a clinical research setting.
  • Over 10 years of experience across clinical monitoring, data management, drug safety, medical monitoring, biometrics, or project management.

Benefits

  • Permanent full-time position
  • Flexible schedule
  • Vacation
  • Home-based position
  • Ongoing learning and development

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