Risk Manager Job: Indero, formerly known as Innovaderm, is a globally recognized clinical research organization (CRO) specializing in dermatology and rheumatology clinical trials. With more than 25 years of experience in clinical research and trial delivery, Indero has built a strong reputation for scientific excellence, operational quality, and innovative study management solutions.
The company supports biotechnology and pharmaceutical sponsors through a comprehensive full-service CRO model that includes protocol design, patient recruitment, clinical monitoring, biometrics, and trial management. With operations spanning North America, Europe, Asia Pacific, and Latin America, Indero continues to expand its global research footprint while maintaining strong collaborations with investigators and patient communities worldwide.
Indero is currently hiring for the position of Risk Manager – India for professionals with strong expertise in clinical research, risk-based monitoring, centralized monitoring, and regulatory compliance.
Risk Manager job– India
- Location: India
- Job Type: Permanent
- Employment Type: Full-Time Professional Role
- Company: Indero
About the Position
The Risk Manager plays a critical role in driving and implementing risk-based monitoring strategies within clinical research projects. The position is focused on ensuring data quality, patient safety, protocol compliance, and overall study integrity through proactive risk identification and mitigation throughout the clinical trial lifecycle.
This role requires close collaboration with cross-functional clinical teams to support the successful execution of Risk-Based Study Management (RBSM) principles. Candidates with strong experience in clinical monitoring, data management, pharmacovigilance, and centralized monitoring processes will be highly suited for this opportunity.
The Risk Manager will also contribute strategic insights for study risk characterization, centralized statistical monitoring, operational oversight, and sponsor communication while ensuring alignment with global regulatory expectations and Good Clinical Practice (GCP) standards.
Key Responsibilities Risk Manager job
The selected candidate will be responsible for the following activities:
- Providing subject matter expertise in developing and updating risk-based monitoring strategies tailored to individual project requirements.
- Collaborating with cross-functional clinical teams to identify, evaluate, and mitigate risks associated with complex clinical trial indications.
- Coordinating with central monitoring teams and reviewing assigned work when required.
- Supporting budget recommendations and managing change orders related to risk management activities.
- Drafting initial risk assessments and supporting the completion of Risk Assessment and Categorization Tools (RACT).
- Assisting Project Managers in transferring identified risks into appropriate tracking systems and ensuring continuous risk review processes.
- Advising teams on functional mitigation plans to effectively address identified risks.
- Utilizing available centralized monitoring tools and remote data review systems to identify potential risks impacting data quality and study integrity.
- Facilitating sponsor and internal review meetings related to findings, escalations, and mitigation strategies.
- Delivering initial and ongoing training sessions to study teams regarding centralized monitoring, risk assessment methodologies, and risk-based monitoring strategies.
- Escalating critical risks, delays, or project deliverables at risk to Project Managers, including changes in project scope.
- Providing strategic input and reporting on risk characterization to leadership teams.
- Taking ownership of additional responsibilities aligned with qualifications, training, and project needs.
Employees may also be assigned additional responsibilities outside their original job description if they possess the necessary qualifications, experience, and training.
Educational Qualification
Candidates applying for this role should possess:
- Bachelor’s degree (B.Pharm, M.Pharma, Pharm D) in a field relevant to Clinical Research or Life Sciences.
Experience Requirements
Applicants should have:
- Minimum 3 years of experience in risk management within a clinical research environment.
- Minimum 5 years of overall experience across:
- Clinical Monitoring
- Data Management
- Drug Safety / Pharmacovigilance
Required Skills & Competencies
The ideal candidate should demonstrate expertise in the following areas:
- Strong understanding of Good Clinical Practice (GCP) and ICH E6 (R3) Guidelines.
- Knowledge of global regulatory requirements applicable to clinical research.
- Experience with Risk-Based Monitoring (RBM) strategies, systems, and operational workflows.
- Advanced proficiency in Microsoft Excel, including sorting, filtering, and pivot tables.
- Expertise in analytical and data visualization tools.
- Familiarity with Lean Six Sigma methodologies and web-based RACT tools.
- Strong analytical thinking and statistical interpretation capabilities.
- Excellent communication, leadership, negotiation, and stakeholder management skills.
- Ability to proactively identify critical risks and develop contingency plans.
- Experience in project workflows and cross-functional team collaboration.
- Training, mentoring, and organizational management capabilities.
- Ability to work independently with a high degree of autonomy.
- Fluent verbal and written English communication skills.
- Ability to communicate effectively across all organizational levels and with external stakeholders.
- Fast learning capability with adaptability to new concepts and systems.
- Strong prioritization and workload management skills in dynamic project environments.
- Excellent understanding of project protocols, centralized monitoring, and risk-based monitoring documentation.
- Broad knowledge of clinical trial processes, functions, and operational activities.
- Experience working with trial management systems or data management systems.
- Good understanding of Health Canada and FDA regulations and guidelines related to clinical research.
Work Environment & Employee Benefits
At Indero, employees work alongside highly skilled and driven professionals in a collaborative and innovation-focused environment. The organization values reliability, responsiveness, and continuous professional growth.
Employees in this position will be eligible for several benefits, including:
- Flexible work schedule
- Permanent full-time employment
- Comprehensive company benefits package
- Ongoing learning and professional development opportunities
- Career advancement possibilities within a global CRO environment
Why Join Indero?
Indero is known globally for its expertise in dermatology and rheumatology clinical research. The company combines scientific excellence with operational efficiency to help pharmaceutical and biotech companies successfully conduct and complete clinical trials worldwide.
With extensive investigator networks, strong patient engagement capabilities, and dedicated research facilities, Indero offers professionals the opportunity to work on impactful global clinical research projects while advancing their careers in a highly specialized CRO environment.
The organization is also committed to equitable treatment, diversity, inclusion, and equal opportunity employment practices. Accommodations are available during the recruitment and selection process for applicants with disabilities upon request.
Eligibility
Applicants must be legally authorized to work in India.
Apply Now
Interested candidates can explore this opportunity and apply directly through the official company website:
