Inductive Quotient Analytics India is hiring Clinical Data Analysts – Clinical Data Management in Hyderabad. The company is looking for professionals with 2+ years of clinical data management experience and hands-on knowledge of EDC systems such as Medidata Rave, Oracle Clinical, Inform, or Veeva.
This is a full-time, onsite opportunity in Hyderabad (Durgamcheruvu) with 2 openings. Candidates with experience in clinical data review, query management, data validation, reconciliation, and clinical database activities can apply.
Job Details
- Company: Inductive Quotient Analytics India
- Position: Clinical Data Analyst – Clinical Data Management
- Experience: 2+ years
- Location: Hyderabad, Telangana
- Work Mode: Onsite
- Employment Type: Full-time, Permanent
- Openings: 2
- Qualification: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Salary: Not disclosed
- Joining Preference: Immediate joiners
About Inductive Quotient Analytics
Inductive Quotient was founded by statisticians and technology industry experts and focuses on advanced digitization, artificial intelligence, machine learning, data science, and analytics solutions for the life sciences industry.
The organization works across statistical and analytical domains and aims to support life sciences organizations through technology-driven solutions.
Clinical Data Analyst – Job Responsibilities
The selected candidate will support end-to-end Clinical Data Management (CDM) activities for clinical trials.
Key responsibilities include:
- Perform clinical data management activities throughout the clinical trial lifecycle.
- Review CRFs and eCRFs for accurate and complete data collection.
- Generate, review, and resolve clinical data queries with investigative sites.
- Perform data cleaning and discrepancy management.
- Conduct data reconciliation activities.
- Validate clinical data for completeness, consistency, and quality.
- Coordinate with Clinical Operations, Biostatistics, Programming, and other cross-functional teams.
- Support database lock and study closeout activities.
- Maintain compliance with ICH-GCP, SOPs, CDISC standards, and applicable regulatory requirements.
- Prepare and maintain clinical data management documentation and reports.
- Participate in User Acceptance Testing (UAT).
- Review and support edit-check testing when required.
Eligibility Criteria
Candidates applying for the Clinical Data Analyst – Clinical Data Management position should have:
- A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline.
- At least 2 years of relevant Clinical Data Management experience.
- Strong understanding of clinical data management processes.
- Experience working with clinical trial data and databases.
- Knowledge of CRF/eCRF review and data validation.
- Experience with query management and discrepancy resolution.
- Understanding of ICH-GCP and clinical trial processes.
- Good communication and cross-functional coordination skills.
- Proficiency in Microsoft Excel and clinical databases.
Preferred Skills
Additional knowledge or experience in the following areas can be advantageous:
- CDISC standards
- SAE reconciliation
- Medical coding
- Clinical study startup
- Clinical study conduct
- Clinical study closeout
- Oncology clinical trials
- EDC systems
- Clinical database validation
EDC Systems Experience
Experience with clinical EDC platforms can be particularly relevant for this role. The job description specifically mentions systems such as:
- Medidata Rave
- Oracle Clinical
- Inform
- Veeva
Professionals familiar with clinical database workflows, data review, query management, edit checks, reconciliation, and database lock activities may find their experience relevant to this position.
Why This Opportunity May Interest Clinical Data Management Professionals
This position provides an opportunity to work on clinical trial data activities while collaborating with functions such as Clinical Operations, Biostatistics, and Programming.
The role can be relevant to professionals looking to further develop experience in:
- Clinical Data Management
- Clinical trial databases
- EDC systems
- Data cleaning and validation
- Query management
- CDISC standards
- Database lock
- Clinical study closeout
- Cross-functional clinical research operations
How to Apply
