Risk Manager at Jobgether – India

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Risk Manager in India.

In this role, you will play a critical part in safeguarding the quality, integrity, and reliability of clinical research data across global clinical trials. You will help design and execute risk-based monitoring strategies that ensure regulatory compliance and support efficient study delivery. Working closely with cross-functional teams, you will identify potential risks early, assess their impact, and drive proactive mitigation plans throughout the clinical trial lifecycle. The position combines strategic oversight with hands-on analytical work, including centralized monitoring and data review. You will act as a key advisor to project teams, helping embed Risk-Based Study Management (RBSM) principles into daily operations. This is a highly collaborative role within a fast-paced, science-driven environment focused on improving patient outcomes and research excellence.

As Risk Manager, you will lead the development and execution of risk-based monitoring frameworks while ensuring consistent oversight of clinical trial data quality and compliance. You will collaborate across functions to identify risks, guide mitigation strategies, and support study teams in implementing effective monitoring approaches.

• Develop, update, and implement risk-based monitoring strategies tailored to study and project requirements.
• Conduct risk assessments and support the creation and maintenance of Risk Assessment and Categorization Tools (RACT).
• Collaborate with cross-functional teams to identify, evaluate, and mitigate risks across clinical trial activities.
• Guide project teams in tracking, documenting, and continuously reviewing identified risks.
• Perform centralized monitoring and remote data reviews using statistical and analytical tools to ensure data integrity.
• Support training initiatives for study teams on risk-based monitoring methodologies and tools.
• Provide input on risk reporting, escalation management, and budget or scope-related changes when required.
• Partner with internal and external stakeholders to ensure alignment on risk mitigation strategies and study delivery.

The ideal candidate has strong experience in clinical research risk management, with a solid understanding of clinical trial operations, regulatory frameworks, and data-driven monitoring approaches. You combine analytical expertise with strong communication and leadership skills, and you are comfortable working in complex, cross-functional environments.

• Bachelor’s degree in a scientific or clinical research-related field.
• Minimum 3 years of experience in risk management within clinical research.
• At least 5 years of experience across clinical monitoring, data management, or drug safety functions.
• Strong knowledge of ICH-GCP (E6 R3), FDA, and Health Canada regulations.
• Experience with Risk-Based Monitoring strategies, centralized monitoring, and RACT tools.
• Proficiency in MS Excel and familiarity with data visualization and analytical tools.
• Understanding of Lean Six Sigma principles and clinical trial management systems.
• Strong analytical, statistical, and problem-solving skills.
• Excellent communication, negotiation, and stakeholder management abilities.
• Ability to manage multiple priorities in a fast-paced, evolving environment.
• Fluent in English, with strong written and verbal communication skills.
• High level of autonomy, adaptability, and ability to learn quickly.

• Flexible work schedule supporting work-life balance
• Permanent full-time employment
• Comprehensive company benefits package
• Continuous learning and professional development opportunities
• Collaborative and innovation-driven work environment
• Global clinical research exposure across multiple regions
• Opportunities to grow within a leading clinical research organization
• Supportive and inclusive workplace culture