Analyst II Clinical Data Manager
Are you searching for high-paying Johnson & Johnson Clinical Data Manager Jobs or J&J Clinical Data Management Recruitment opportunities? The global healthcare innovator, Johnson & Johnson, has announced openings for the position of Analyst II Clinical Data Manager based at its offices in Hyderabad, Bangalore, and Mumbai, India.
This role operates under a hybrid model and is ideal for data professionals with a minimum of 2 years of experience in Clinical Data Management (CDM), pharmaceutical, or CRO environments. If you want to understand how CDM stacks up against clinical analytics, read our detailed comparison on Clinical SAS vs Clinical Data Management.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Analyst II Clinical Data Manager |
| Company | Johnson & Johnson (J&J) |
| Department | Data Analytics & Computational Sciences – CDM |
| Location | Hyderabad, Bangalore & Mumbai, India |
| Work Mode | Hybrid |
| Experience Required | 2+ Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BSc/MSc, B.Tech Biotech, BE/B.Tech (CS) |
| Application Deadline | June 30, 2026 |
💼 Key Responsibilities
Clinical Data Management & Oversight
- Provide operational oversight and accountability for clinical data management activities across multiple trials.
- Review requirements for eCRF layouts and study-specific electronic data collection tools.
- Establish clinical data standards, conventions, and data quality metrics for projects.
- Define database dataset structure, dictionary requirements, and edit check parameters.
- Monitor database timelines and ensure on-time delivery of database lock milestones.
Documentation, Compliance & Audits
- Review and edit data management documents and regulatory submission packages.
- Ensure complete quality compliance, database validation accuracy, and GCP documentation standards.
- Maintain real-time inspection readiness for all trial databases and study files.
- Participate in and support internal QA audits and external regulatory agency inspections.
Scientific Data Review & Collaboration
- Manage Study Responsible Scientist (SRS) and Study Responsible Physician (SRP) queries within EDC tools.
- Conduct scientific data reviews of complex clinical trial data sets.
- Collaborate with global biostatisticians, clinical teams, medical writers, and CRO partners.
- Perform adverse event coding validation, SAE reconciliation, and functional data reviews.
🎓 Qualifications & Eligibility
Candidates with the following educational background are eligible:
- B.Pharm, M.Pharm, or Pharm.D
- B.Sc or M.Sc in Life Sciences (Biotechnology, Biochemistry, Microbiology, etc.)
- B.Tech or M.Tech in Biotechnology
- B.E / B.Tech in Computer Science (with pharma domain knowledge)
- Bachelor’s, Master’s, or PhD in Health Sciences or related disciplines
For pharmacy graduates planning to transition into international regulatory or clinical domains, read our guide on B.Pharm Career Opportunities: India vs USA.
🧠 Preferred Skills
- Experience working with Electronic Data Capture (EDC) systems (Rave, Inform, Oracle Clinical).
- Understanding of Good Clinical Practice (GCP), clinical operations, and data privacy regulations.
- Experience coordinating database builds, edit checks, and validation setups.
- Analytical thinking, biostatistics familiarity, and advanced report writing capabilities.
- Excellent written and verbal English communication and problem-solving abilities.
If you want to evaluate your healthcare analytics readiness, take our Healthcare Data Analyst Quiz. To prepare for upcoming interviews, read our guide to master your data analyst interview.
💰 Salary & J&J Employee Benefits
J&J provides premium compensation matching the experience level of candidates:
Estimated Salary Range: ₹9,00,000 – ₹16,00,000 Per Annum (CTC)
Benefits
- Opportunity to work on global, high-impact clinical trials.
- Flexible, hybrid work environment.
- Access to advanced computational science and clinical database technologies.
- Continuous corporate learning, development, and leadership programs.
- Inclusive workplace culture with comprehensive employee wellness initiatives.
🌟 Why Join Johnson & Johnson?
- J&J is one of the world's most respected and innovative healthcare giants.
- Direct involvement in clinical trials that bring transformational medicines to market.
- Work with global cross-functional clinical development and regulatory affairs teams.
If you want to read more about operations roles in trials, check our detailed Clinical Research Coordinator (CRC) Guide.
📑 Resume Tips
- Detail your experience managing clinical trials and database milestones.
- Highlight your proficiency with EDC platforms (especially Medidata Rave).
- State your experience in collaborating with international vendors and CROs.
- Keep your resume layout clean, ATS-compliant, and professional.
🎯 Interview Questions
- What are the primary responsibilities of a Lead Clinical Data Manager on a study?
- How do you ensure clinical database inspection readiness during study execution?
- Explain your workflow for reconciling Serious Adverse Events (SAEs) between safety and clinical databases.
- How do you manage database build and data validation timeline delays with CRO vendors?
- What is an Integrated Review Plan, and what role does it play in scientific data review?
📌 How to Apply?
Interested candidates who fulfill the eligibility parameters can apply online by visiting J&J's official career portal. The deadline to submit applications is June 30, 2026. To prepare your profile and optimize your registration, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
The deadline to submit applications on the J&J portal is June 30, 2026.
Q. Where are these roles located?
The Analyst II CDM position is based at J&J's offices in Hyderabad, Bangalore, and Mumbai on a hybrid work model.
Q. What experience range is suitable?
Johnson & Johnson is seeking candidates with at least 2 years of clinical data management experience.
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