IQVIA is hiring experienced Centralized Monitoring professionals in Hyderabad for full-time hybrid opportunities. This opening is suitable for clinical research professionals with hands-on experience in Centralized Monitoring, Risk-Based Monitoring (RBM), and Data-Driven Monitoring (DDM).
Candidates should have at least 3 years of clinical research experience, including a minimum of 2 years of Centralized Monitoring experience. Immediate joiners are preferred.
This IQVIA Hyderabad job offers an opportunity to work in a technology-driven clinical research environment supporting risk-based oversight and centralized clinical trial monitoring.
Job Overview
| Details | Information |
|---|---|
| Company | IQVIA |
| Position | Centralized Monitoring Professional |
| Industry | Clinical Research / Life Sciences |
| Location | Hyderabad |
| Employment | Full-time |
| Work Mode | Hybrid – 4 days from office |
| Overall Experience | 3+ years in Clinical Research |
| Centralized Monitoring Experience | Minimum 2+ years |
| Key Skills | Centralized Monitoring, RBM, DDM |
| Joining Preference | Immediate Joiners Preferred |
Key Responsibilities
Based on the skills specified for the opening, selected professionals may be responsible for:
- Supporting centralized monitoring activities for clinical trials.
- Reviewing clinical study data to identify potential risks, trends, anomalies, and data-quality concerns.
- Applying Risk-Based Monitoring (RBM) methodologies to support effective clinical trial oversight.
- Performing Data-Driven Monitoring (DDM) activities using available study and operational data.
- Identifying potential site-level or study-level risks requiring further investigation.
- Collaborating with clinical operations and other cross-functional study teams.
- Supporting risk identification, tracking, escalation, and resolution processes.
- Maintaining appropriate documentation related to centralized monitoring activities.
- Contributing to quality and compliance throughout clinical study execution.
Qualifications and Experience
Candidates interested in IQVIA Centralized Monitoring jobs in Hyderabad should meet the following requirements:
- 3+ years of experience in a clinical research background.
- Minimum 2+ years of hands-on Centralized Monitoring experience.
- Strong experience and understanding of Risk-Based Monitoring (RBM).
- Experience with Data-Driven Monitoring (DDM).
- Knowledge of clinical research and clinical trial processes.
- Ability to review and interpret clinical and operational study data.
- Strong analytical, communication, and problem-solving skills.
- Immediate joiners are preferred.
Qualification Note: The hiring notice does not specify a particular academic degree. Candidates should confirm educational eligibility directly with the IQVIA recruitment team before applying.
Why Consider This IQVIA Opportunity?
This opening can be relevant for experienced clinical research professionals looking to strengthen their careers in centralized and risk-based clinical trial monitoring.
Potential advantages include:
- Opportunity to work with IQVIA, a major organization in the clinical research and healthcare sector.
- Exposure to Centralized Monitoring methodologies.
- Experience working with RBM and DDM approaches.
- Hybrid working arrangement.
- Opportunity to work within multidisciplinary clinical research teams.
- Career exposure to technology-enabled clinical trial oversight.
How to Apply
Eligible candidates can apply by sharing their updated CV directly with the recruiter mentioned in the hiring announcement.
Send CV to: ashwini.veerabhadrappa@iqvia.com
Candidates should highlight their Centralized Monitoring, RBM, DDM, and overall clinical research experience clearly on their resume.