Senior Central Monitor Job in India at Indero for experienced clinical research professionals with RBQM and statistical data analytics expertise.
Job Title: Senior Central Monitor
Company: Indero
Job Location: India
Experience Required: 8 Years Overall (Minimum 3 Years in Central Statistical Monitoring)
Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
Employment Type: Full-Time, Permanent
Application Mode: Online Application
Job Status: Verified
🔷 Key Highlights
- Verified Senior-Level Central Monitoring Job in India
- Full-Time Permanent Position
- Minimum 8 Years of Clinical Research Experience Required
- Strong Exposure to Centralized Statistical Monitoring and RBQM
- Opportunity to Work with a Global Dermatology-Focused CRO
- Flexible and Nontraditional Work Environment
- Advanced Role in Risk-Based Monitoring and Clinical Data Analytics
- Global Project Exposure with International Research Teams
📌 About Indero CRO
Indero is a globally reputed Contract Research Organization (CRO) with a strong specialization in dermatology-focused clinical research. Established in 2000 and headquartered in Montreal, Indero has steadily expanded its presence across North America and Europe. The organization supports biopharmaceutical sponsors with high-quality clinical operations, data management, biometrics, and centralized monitoring solutions.
With over two decades of expertise in dermatology and inflammatory disease research, Indero is known for scientific innovation, regulatory compliance, and patient-centric clinical development. The organization delivers end-to-end clinical research services while maintaining the highest standards in Good Clinical Practice (GCP), data integrity, and regulatory quality.
Indero promotes an inclusive workplace culture and equal-opportunity employment practices. Professionals joining Indero gain access to cutting-edge centralized monitoring platforms, global research exposure, and long-term career advancement in clinical research operations.
🧪 About the Role – Senior Central Monitor
The Senior Central Monitor role at Indero is a high-impact leadership position within the centralized monitoring and clinical data analytics function. This role is designed for experienced clinical research professionals who have extensive hands-on expertise in central statistical monitoring, Risk-Based Quality Management (RBQM), and advanced clinical data review.
As a Senior Central Monitor, you will play a critical role in identifying emerging data quality risks, assessing trial performance, detecting safety and operational anomalies, and driving proactive risk mitigation strategies across multi-country clinical trials. You will also mentor junior central monitoring staff and represent the centralized monitoring function in cross-functional study risk management forums.
This is a strategic role for professionals seeking to advance into senior leadership positions within centralized monitoring, clinical operations, and data-driven clinical quality management.
📝 Detailed Job Responsibilities
As a Senior Central Monitor at Indero, your responsibilities will include:
- Leading the setup and development of study-specific centralized monitoring plans
- Designing and configuring customized analysis tools for centralized review
- Conducting centralized statistical reviews of accumulating clinical study data
- Identifying emerging trends, data outliers, safety signals, and performance variability
- Assessing site-level and country-level risks through analytics-driven monitoring
- Preparing centralized monitoring dashboards and risk summary reports
- Delivering regular centralized monitoring presentations to study teams
- Facilitating and leading risk review meetings with cross-functional stakeholders
- Coordinating project timelines and overseeing on-time delivery of analysis outputs
- Assigning analytical tasks to team members and monitoring workload distribution
- Training and mentoring junior central monitors on methodologies and tools
- Representing the centralized monitoring team during RBQM and operational governance meetings
- Supporting operational tasks such as database updates, reports generation, and review configurations
- Ensuring proactive communication and escalation of identified risks
- Managing data quality issues and tracking corrective and preventive actions (CAPAs)
- Supporting inspection readiness and audit preparation activities
- Ensuring compliance with GCP, regulatory requirements, and internal SOPs
This role requires a strong combination of analytical expertise, leadership capability, cross-functional coordination, and regulatory awareness.
🎓 Educational Qualifications
To be eligible for this position, candidates must hold one of the following qualifications:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Doctor of Pharmacy (Pharm.D)
- Master of Science (MSc)
- Bachelor of Science (BSc)
- Any recognized degree in Life Sciences, Clinical Research, Biotechnology, or Biomedical Sciences
Candidates with clinical research certifications and advanced training in data analytics or RBQM will have an added advantage.
✅ Experience & Technical Skill Requirements
Candidates must meet the following experience and skill criteria:
- Minimum 3 years of proven hands-on experience in central statistical monitoring
- Total overall experience of at least 8 years in clinical research operational domains such as:
- Clinical monitoring
- Data management
- Pharmacovigilance and drug safety
- Medical monitoring
- Biometrics
- Project management
- Strong knowledge of Risk-Based Quality Management (RBQM) principles and implementation
- Demonstrated experience analyzing clinical trial data for quality trends and performance risks
- Familiarity with core clinical systems such as EDC, IRT, CTMS
- Advanced proficiency in Microsoft Excel, Word, and PowerPoint
- Sound understanding of descriptive statistical methods including means, medians, variability measures, and confidence intervals
- Ability to work in flexible and nontraditional work environments
🧠 Key Behavioral & Professional Attributes
Successful candidates will demonstrate the following professional attributes:
- Excellent written and verbal English communication skills
- Strong analytical and critical thinking ability
- High learning agility and adaptability
- Exceptional prioritization and workload management capability
- Solid understanding of end-to-end clinical trial processes
- In-depth awareness of GCP guidelines and regulatory expectations
- Strong coordination capability across data management, clinical operations, and biometrics teams
- Leadership mindset with coaching and mentoring capabilities
- High level of professionalism and confidentiality in handling clinical data
🏙️ Job Location – India
This is a full-time permanent role open to candidates across India. The flexibility of work location allows experienced professionals to contribute to global dermatology trials while maintaining a balanced professional lifestyle.
This opportunity is highly suitable for senior professionals seeking growth in centralized monitoring, global clinical operations, and analytics-driven quality oversight.
📈 Career Growth & Global Exposure
This Senior Central Monitor position at Indero offers exceptional long-term career growth potential. You will gain:
- Strategic exposure to global dermatology-focused clinical research programs
- Leadership experience in centralized monitoring operations
- Advanced expertise in RBQM implementation and risk governance
- Cross-functional exposure with global project teams
- Opportunities to progress into associate director or centralized monitoring lead roles
- Continuous professional development through advanced training initiatives
- Long-term stability in a specialized clinical research domain
This role is ideal for professionals looking to transition into advanced clinical analytics, quality oversight leadership, and global research governance careers.
💼 Benefits of Working at Indero
Indero offers a highly competitive and professional work environment with strong employee benefits, including:
- Permanent full-time employment
- Flexible work schedules
- Supportive and collaborative team environment
- Continuous professional learning and skills enhancement
- Exposure to high-quality global dermatology trials
- Access to advanced centralized monitoring platforms
- Opportunity to influence global clinical quality strategies
- Long-term career security within a specialized CRO
📊 Senior Central Monitor Job Summary
| Category | Details |
|---|---|
| Job Title | Senior Central Monitor |
| Company | Indero CRO |
| Job Location | India |
| Experience | 8 Years Overall |
| Central Monitoring Experience | Minimum 3 Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences |
| Employment Type | Full-Time, Permanent |
| Application Mode | Online Application |
| Industry | Clinical Research, Central Monitoring, RBQM |
| Job Status | Verified |
🔍 Who Should Apply for This Role?
This opportunity is best suited for:
- Senior clinical research professionals
- Central statistical monitoring specialists
- RBQM experts
- Clinical data analytics professionals
- Biometrics and data quality specialists
- Experienced CRAs transitioning to centralized monitoring
- Project managers with strong data review expertise
- Global clinical operations professionals
If you have extensive experience in clinical data oversight, centralized risk monitoring, and regulatory-quality frameworks, this role offers outstanding career value.
⚠️ Important Notes for Applicants
- This is a senior-level role and freshers are not eligible
- Only candidates meeting experience criteria should apply
- Applications without central monitoring experience may not be shortlisted
- Selected candidates will go through technical interviews and analytics assessments
- All applications will be handled confidentially
📝 How to Apply (Final Section)
Interested and eligible candidates can apply online for the Senior Central Monitor position at Indero by following the steps below:
- Visit the official Indero career portal
- Search for the opening titled “Senior Central Monitor – India”
- Carefully review the complete job description and eligibility criteria
- Click on the “Apply Now” button
- Create your profile or log in to your existing account
- Upload your updated resume with detailed centralized monitoring experience
- Complete the application form with accurate professional details
- Submit your application successfully
- Wait for further communication from the recruitment team
✅ Shortlisted candidates will be contacted via email for technical interviews and further evaluation.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
