Novotech Hiring Clinical Data Associate I | Bangalore CRO Jobs 2026
Are you looking for Novotech Careers Bangalore or Clinical Data Associate CRO Jobs India? Global CRO leader Novotech is hiring a Clinical Data Associate I at its Bangalore, Karnataka office to support clinical trial data management operations.
This entry-level CDM opportunity is ideal for fresh pharmacy and life sciences graduates with 6 months to 1 year of experience in clinical research, CDM, or CRO environments. To craft a strong CDM-focused resume and begin your journey in clinical data management, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Novotech |
| Position | Clinical Data Associate I |
| Job ID | 4127 |
| Job Location | Bangalore, Karnataka, India |
| Department | Clinical Data Management (CDM) |
| Employment Type | Full-Time |
| Experience Required | 6 Months – 1 Year Preferred |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotechnology, Nursing, Life Sciences |
| Estimated Salary | As Per Industry Standards |
| Last Date to Apply | July 2, 2026 |
💼 Key Responsibilities
- Perform clinical trial data entry using Clinical Data Management (CDM) software and Electronic Data Capture (EDC) systems.
- Validate clinical data for completeness, accuracy, and consistency in line with study protocols.
- Review, process, and resolve data queries raised during clinical trials.
- Track Case Report Forms (CRFs) and maintain query logs and study tracking reports.
- Assist Clinical Data Managers (CDMs) in database setup, testing, and edit check validation.
- Perform external data reconciliation and coordinate electronic data transfers.
- Generate reports, data listings, and summaries during clinical studies.
- Coordinate coding activities including medical term coding using MedDRA and WHO Drug Dictionary.
- Support study progress tracking systems and participate in project meetings.
- Prepare meeting agendas and minutes for CDM team discussions.
- Maintain compliance with ICH-GCP guidelines, GCDMP, and company SOPs.
- Contribute to process improvement initiatives within the CDM department.
To understand how clinical data management roles compare to clinical trial monitoring and medical writing careers at a CRO, read our guide on B.Pharm Careers after Graduation: India vs USA.
🎓 Required Qualifications & Skills
- Education: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotechnology, Microbiology, Biochemistry, Nursing, Clinical Research, or Allied Health Sciences.
- Experience: 6 months to 1 year in Clinical Research, CRO, Pharmaceutical, or Healthcare industries preferred. Fresh graduates with relevant CDM internships may also be considered.
- Technical Skills: Knowledge of CDM processes, CRF review, query management, database validation, and EDC systems (Medidata Rave, Oracle InForm, or similar).
- Regulatory Knowledge: Familiarity with ICH-GCP guidelines, Good Clinical Data Management Practice (GCDMP), and Good Documentation Practices.
- Computer Skills: Proficiency in Microsoft Excel, Word, and PowerPoint.
To assess your clinical trial and GCP knowledge before this interview, try our interactive Clinical Trial Assistant (CTA) Quiz.
🎁 Why Join Novotech?
- Work with a globally respected CRO with 30+ offices and expertise across Asia-Pacific, Europe, and North America.
- Flexible working options and supportive wellness programs.
- Paid parental leave and continuous learning & development opportunities.
- Exposure to diverse international clinical research projects across multiple therapeutic areas.
- Professional mentorship and clear career progression pathways in CDM.
To compare CRO clinical data management salaries in India versus the US, read our in-depth report on Pharmacovigilance Salary: India vs USA.
💡 Clinical Data Management vs Healthcare IT
Clinical Data Associates manage trial data, CRF review, and database validation to ensure data quality in clinical studies, whereas Healthcare IT professionals maintain the technical infrastructure and software platforms behind these systems. To understand these distinct career paths, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Novotech Clinical Data Associate
- Highlight EDC Experience: Mention any hands-on or academic exposure to EDC platforms like Medidata Rave, Oracle InForm, OpenClinica, or similar CDM tools — even from internships or training programs.
- Showcase Data Management Projects: Highlight academic or professional projects involving data entry, validation, or clinical data review — especially any CRF design or query resolution experience.
- Emphasize Regulatory Competencies: Include knowledge of ICH-GCP, GCDMP, and Good Documentation Practices to demonstrate your understanding of clinical data compliance standards.
- Quantify Your Skills: Mention specific tools, databases, or therapeutic areas you have worked with to make your resume stand out against other candidates.
💬 Novotech Clinical Data Associate Interview Questions
- Q1. What is the difference between a CRF and an eCRF?
Answer Guidance: A CRF (Case Report Form) is a paper-based document used to collect clinical trial data. An eCRF (electronic CRF) is a digital version captured via EDC systems like Medidata Rave, reducing transcription errors and enabling real-time data access. - Q2. What is a data query in clinical data management and how is it resolved?
Answer Guidance: A data query is a discrepancy or inconsistency in clinical trial data flagged by the CDM team. It is resolved by coordinating with the site investigator or CRA to clarify, correct, or confirm the data, followed by formal query closure in the system. - Q3. What are edit checks and why are they important in CDM?
Answer Guidance: Edit checks are programmed validation rules built into the EDC system to automatically detect data entry errors, missing values, or protocol deviations. They ensure data quality and reduce manual query generation during the trial.
🚀 How to Apply?
Eligible candidates can apply directly via Novotech's official Oracle Cloud HCM careers portal. Click the button below:
Apply Online – Novotech Careers Portal⏰ Last Date to Apply: July 2, 2026
❓ Frequently Asked Questions
Q. Are freshers eligible for this Novotech Clinical Data Associate role?
Fresh graduates with relevant CDM internships or academic research exposure may be considered depending on project requirements.
Q. What is the work location for this position?
This is a full-time, office-based position at Novotech's Bangalore, Karnataka office.
Q. What is the last date to apply for this role?
The last date to apply for the Novotech Clinical Data Associate I role is July 2, 2026. Apply at the earliest to avoid missing the deadline.
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