Indero Hiring Central Monitor in India – Work From Home
Indero is recruiting for the position of Central Monitor in India. This is a permanent, full-time, home-based opportunity for experienced clinical research professionals with a relevant bachelor’s degree, at least 1 year of central statistical monitoring experience, and 6 years of overall experience across two or more clinical research operational areas.
The role focuses on centralized clinical trial data review, statistical monitoring, risk-based quality management, and identifying potential data quality issues across clinical studies, countries, and sites. Professionals with experience in clinical monitoring, clinical data management, drug safety, biometrics, or project management may be suitable if they meet the specific experience requirements.
Job Details
| Particulars | Details |
|---|---|
| Company | Indero |
| Position | Central Monitor |
| Job Type | Permanent, full-time |
| Location | India – Home-based |
| Qualification | Bachelor’s degree in a field relevant to clinical research |
| Experience | 1 year in central statistical monitoring and 6 years overall across at least 2 operational areas |
| Key Skills | Centralized monitoring, clinical data review, RBQM, EDC, IRT, CTMS, Microsoft Office |
| Work Arrangement | Remote |
| Application | Official Indero careers portal |
About Indero
Indero is a Contract Research Organization (CRO) specializing in dermatology and rheumatology clinical research. The company supports pharmaceutical and biotechnology sponsors with clinical trial services, including protocol development, patient recruitment, trial monitoring, and biometrics.
The Central Monitor position supports clinical trial quality by reviewing accumulating study data remotely, identifying unusual trends and potential risks, and helping study teams address data integrity concerns.
Roles and Responsibilities
The Central Monitor conducts centralized reviews of clinical trial and operational data throughout the study lifecycle, from study initiation through database lock.
Key responsibilities include:
- Reviewing clinical trial subject and operational data according to the centralized monitoring plan.
- Using analytical tools and clinical systems to identify data quality trends, unusual variability, outliers, and potential study risks.
- Identifying possible systematic errors and performance issues at the study, country, or site level.
- Documenting monitoring reviews and findings according to established procedures.
- Supporting the central monitoring team in completing assigned reviews accurately and within deadlines.
- Providing input to senior team members on risk characterization and monitoring reports.
- Supporting review setup, maintaining departmental databases, and generating reports as assigned.
- Contributing to data quality oversight across clinical studies, countries, and sites.
- Communicating potential risks and relevant findings to appropriate team members.
Eligibility Criteria
Educational Qualification
A bachelor’s degree in a field relevant to clinical research is required.
Relevant academic backgrounds may include:
B.Pharm | M.Pharm | Pharm.D | B.Sc Life Sciences | M.Sc Life Sciences | Biotechnology | Microbiology | Biochemistry | Clinical Research | Nursing
These are examples of potentially relevant fields; the employer does not explicitly confirm every degree listed above. Candidates should ensure their qualification meets Indero’s stated requirement.
Experience Requirements
This is an experienced-level clinical research position. Candidates must meet both of the following requirements:
- At least 1 year of experience in central statistical monitoring.
- At least 6 years of overall experience across two or more clinical research operational areas, such as clinical monitoring, data management, drug safety, medical monitoring, biometrics, or project management.
Candidates should also have experience reviewing clinical data and using clinical trial management or data management systems.
Technical Knowledge and Skills
The employer highlights the following requirements:
- Basic understanding of statistical monitoring and Risk-Based Quality Management (RBQM).
- Knowledge of clinical study management, data management, and regulatory operations.
- Familiarity with clinical trial systems such as Electronic Data Capture (EDC), Interactive Response Technology (IRT), and Clinical Trial Management Systems (CTMS).
- Good knowledge of Microsoft Word, Excel, and PowerPoint.
- Basic understanding of descriptive statistics, including means, medians, significance, and confidence intervals.
- Ability to extract relevant information from study protocols and electronic clinical trial systems.
- Understanding of Good Clinical Practice (GCP) and applicable Health Canada and US FDA regulations and guidelines.
- Strong analytical thinking, communication, prioritization, and time-management skills.
- Excellent written and spoken English.
Work Location and Benefits
This is a home-based position in India. Indero notes that attendance at some meetings outside regular business hours, primarily in the evening, is required.
The employer lists the following benefits:
- Flexible work schedule.
- Permanent, full-time employment.
- Ongoing learning and development opportunities.
Applicants must be legally eligible to work in India.
How to Apply for Indero Jobs
Candidates who meet the educational and experience requirements can apply through the official Indero careers website.
Apply online: https://inderocro.com/careers-2/co/india/F7.473/central-monitor-india/all/?coref=1.11.p05_7D18
Before applying, highlight your central statistical monitoring experience, clinical data review, RBQM knowledge, clinical systems expertise, and experience across relevant clinical research functions.
Job Summary
| Category | Details |
|---|---|
| Company | Indero |
| Position | Central Monitor |
| Qualification | Relevant bachelor’s degree |
| Experience | 1 year in central statistical monitoring plus 6 years overall across 2 or more operational areas |
| Location | India – Home-based |
| Job Type | Permanent, full-time |
| Key Skills | Central monitoring, RBQM, clinical data review, EDC, CTMS |
| Fresher Eligibility | Not eligible |
| Apply | Official Indero careers portal |
Disclaimer: Job details and eligibility criteria are based on the supplied recruitment announcement. Candidates should verify that the vacancy remains open and confirm all requirements on the official careers website before applying.