Novotech Hiring Clinical Data Associate, Senior CDA & Team Lead – Bengaluru
Are you searching for Clinical Data Management Jobs in India, Clinical Data Associate careers in Bengaluru, or Senior CDM vacancies at a global CRO? One of the world's leading Contract Research Organizations, Novotech, is now hiring for three specialized positions in its Biometrics and Clinical Data Management department at its Bengaluru office.
This electronic data capture (EDC) operations, query management, CRF reconciliation, database validation, User Acceptance Testing (UAT), and ICH-GCP compliant clinical data oversight vacancy covers three progressive career levels: Clinical Data Associate (1–2 years), Senior Clinical Data Associate (2–4 years), and Team Lead – Clinical Data Management (4–6 years). Candidates holding degrees in Pharmacy, Life Sciences, Biological Sciences, Clinical Sciences, or Mathematical Sciences are encouraged to apply. To write a focused, ATS-optimized resume highlighting your EDC platform experience, clinical database knowledge, or team coordination achievements, review our guide on how to apply for healthcare and pharma jobs online.
📋 Job Overview
- Company: Novotech
- Industry: Clinical Research / Contract Research Organization (CRO)
- Department: Biometrics / Clinical Data Management
- Job Location: Bengaluru, Karnataka, India
- Employment Type: Full-Time
- Total Open Positions: 3
- Experience Required: 1–6 Years (Role Dependent)
- Qualifications: B.Sc / M.Sc / B.Pharm / M.Pharm / Pharm.D / Life Sciences / Clinical / Biological / Mathematical Sciences
- Work Mode: On-site
💼 Available Positions & Responsibilities
1. Clinical Data Associate (1–2 Years Experience)
- Perform clinical trial data entry and review using EDC systems.
- Track CRF receipt, completion status, and missing data.
- Perform query management activities and data cleaning.
- Support database testing, edit check validation, and UAT activities.
- Assist in external data reconciliation from lab or third-party vendors.
- Generate study listings, reports, and metric summaries.
- Maintain all study documentation in compliance with SOPs and ICH-GCP.
2. Senior Clinical Data Associate (2–4 Years Experience)
- Independently manage end-to-end clinical trial data review activities.
- Prepare and validate database specifications and edit check programs.
- Conduct User Acceptance Testing (UAT) independently.
- Perform external data reconciliation and third-party vendor coordination.
- Archive study documentation and lead CDA process improvement initiatives.
- Mentor junior Clinical Data Associates and support Clinical Data Managers.
- Participate in investigator meetings and cross-functional project review calls.
3. Team Lead – Clinical Data Management (4–6 Years Experience)
- Lead and manage Clinical Data Management project teams across multiple trials.
- Oversee resource planning, allocation, and performance management activities.
- Review and approve Data Management Plans (DMPs) and SOPs.
- Participate in proposal development and budget planning support.
- Ensure all CDM operations maintain full ICH-GCP and GCDMP regulatory compliance.
- Mentor senior and junior team members, support career development planning.
To understand how Clinical Data Management compares with SAS programming and CDISC dataset submission careers, read our analysis on Clinical SAS vs Clinical Data Management.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Life Sciences, Clinical Sciences, Pharmacy (B.Pharm, M.Pharm, Pharm.D), Biological Sciences, or Mathematical Sciences.
- Experience: 1 to 6 years in clinical data management, EDC operations, or clinical research biometrics.
- Key Technical Skills: EDC platforms, CRF review, query management, data validation, database reconciliation, CDISC knowledge (preferred).
- Guidelines Knowledge: Strong understanding of ICH-GCP, GCDMP, and regulatory data compliance frameworks.
- Soft Skills: Strong analytical ability, attention to detail, written communication, and team collaboration.
To review core concepts of SDTM, ADaM, and CDISC standards expected in CDM interviews, explore our dedicated guide on CDISC SDTM & ADaM Overview.
🎁 Why Join Novotech?
- Work on global multinational clinical trials across diverse therapeutic areas.
- Competitive salary packages with structured annual appraisal cycles.
- Flexible working policies and comprehensive wellness initiatives.
- Paid parental leave and generous leave entitlement policies.
- Dedicated professional training programs and career development pathways.
- Diversity and inclusion-driven workplace culture.
📝 Resume Tips for Novotech CDM Candidates
- List EDC Platforms: Mention specific EDC systems you have worked with (e.g., Medidata Rave, Oracle InForm, Veeva Vault EDC).
- Detail Study Experience: Include the number of studies managed, therapeutic areas covered, and team size supervised.
- Use CDM Keywords: Include terms like Query Management, CRF Reconciliation, Database Lock, UAT, GCDMP, and CDISC in your resume.
💬 Novotech Clinical Data Management Interview Questions
- Q1. What is a Data Management Plan (DMP) and what does it typically include?
Answer Guidance: A DMP is a key clinical trial document that outlines the data management procedures for a specific study. It typically includes database design, data entry guidelines, edit check specifications, query management rules, external data reconciliation procedures, and database lock criteria, all aligned with ICH-GCP and GCDMP standards. - Q2. Explain the difference between a programmatic edit check and a manual data review.
Answer Guidance: A programmatic edit check is an automated rule built into the EDC system that triggers a query whenever entered data fails validation (e.g., out-of-range lab values). A manual data review is performed by a CDM professional who visually inspects data for contextual inconsistencies, missing entries, or protocol deviations that automated rules may not detect. - Q3. What steps are involved in database lock?
Answer Guidance: Database lock involves resolving all outstanding queries, completing external data reconciliation, completing edit check validation, getting sign-off from the CDM team and investigator, performing a final data review, freezing the database to prevent further changes, and documenting the lock in the trial master file (TMF).
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to navigate corporate recruitment portals and format your details:
🔗 Direct Application Links (All 3 Positions)
Click on the relevant button below to apply directly on Novotech's official recruitment portal:
📋 Apply – Clinical Data Associate 📋 Apply – Senior Clinical Data Associate 📋 Apply – Team Lead, Clinical Data Management📄 Try Free ATS Resume Analyzer & Builder
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🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. Can freshers with less than 1 year of experience apply for the CDA role at Novotech?
The Clinical Data Associate role prefers 1–2 years of experience. Candidates with relevant internships, academic projects in EDC or clinical data, or equivalent exposure may be considered.
Q. Is CDISC knowledge mandatory for these positions?
CDISC knowledge is listed as preferred, not mandatory, for the CDA and Senior CDA roles. However, it is an important advantage, especially for those applying to the Senior CDA or Team Lead position.
Q. What is the work mode for these Novotech Bengaluru positions?
All three positions are full-time, onsite roles based at Novotech's Bengaluru office in Karnataka.
