Indero, a globally recognized dermatology-focused CRO, is hiring a Senior Central Monitor in India. This is a high-impact, full-time role for experienced clinical research professionals skilled in central statistical monitoring, RBQM, clinical data analytics, and risk-based monitoring strategies.
If you have strong expertise in clinical operations, data management, and centralized monitoring, this opportunity offers a fast-paced, flexible work environment with global exposure.
Key Responsibilities
As a Senior Central Monitor, you will:
- Lead the setup of study-specific analysis tools and centralized monitoring plans.
- Conduct centralized statistical review of accumulating study data.
- Identify emerging data quality risks, trends, outliers, and variability using analytics.
- Deliver centralized monitoring reports and conduct risk review meetings.
- Coordinate timelines, assign analysis tasks, and ensure on-time completion of deliverables.
- Train and mentor junior staff on centralized monitoring methodologies.
- Represent the central monitoring team during cross-functional risk assessment meetings.
- Support operational activities such as updating databases, pulling reports, and review setup.
- Ensure proactive communication, escalation, and management of study risks across sites/countries.
Qualifications & Experience
To succeed in this role, candidates must have:
Education
- Bachelor’s degree in a field relevant to clinical research (Life Sciences, Pharmacy, Biotechnology, etc.)
Experience
- Minimum 3 years in central statistical monitoring.
- Overall 8 years in operational areas such as:
- Clinical monitoring
- Data management
- Pharmacovigilance / Drug safety
- Medical monitoring
- Biometrics
- Project management
- Strong knowledge of RBQM (Risk-Based Quality Management) and its impact on data integrity.
- Experience analyzing clinical study data and identifying quality trends.
- Familiarity with systems like EDC, IRT, CTMS.
- Advanced proficiency in MS Office (Excel, Word, PowerPoint).
- Understanding of descriptive statistical methods (means, medians, confidence intervals).
- Ability to work in nontraditional or flexible work environments.
Attributes
- Excellent English communication skills (written and verbal).
- Fast learner with strong prioritization and workload management skills.
- Solid understanding of clinical trial processes and GCP guidelines.
- Effective time management and cross-functional coordination capabilities.
Benefits of Working at Indero
- Permanent full-time position
- Flexible work schedule
- Supportive and collaborative environment
- Opportunities for growth in centralized monitoring
- Continuous learning and development
- Work with global dermatology-focused research teams
About Indero
Indero is a leading Contract Research Organization (CRO) specializing in dermatology research since 2000. Headquartered in Montreal, the organization continues to expand across North America and Europe. Known for high-quality research and innovation, Indero offers an inclusive workplace and equal-opportunity recruitment practices.
