Global healthcare leader Johnson & Johnson (J&J) has announced openings for the position of Analyst II Clinical Data Manager in Hyderabad, Bangalore, and Mumbai, India. The company is seeking professionals with at least 2 years of experience in Clinical Data Management (CDM), pharmaceutical, CRO, or biotech industries.
This is an excellent opportunity for clinical data management professionals looking to work with one of the world’s most respected healthcare organizations and contribute to innovative clinical development programs.
Job Details
- Position: Analyst II Clinical Data Manager
- Company: Johnson & Johnson
- Department: Data Analytics & Computational Sciences – Clinical Data Management
- Job Type: Full-Time
- Work Mode: Hybrid
- Locations: Hyderabad, Bangalore, Mumbai, India
- Application Deadline: June 30, 2026
- Experience Required: 2+ Years
- Industry: Pharmaceutical, CRO, Biotechnology
About the Role
The Analyst II Clinical Data Manager will provide oversight and accountability for clinical data management activities across multiple clinical trials. The role involves managing data quality, coordinating with cross-functional stakeholders, ensuring regulatory compliance, and supporting scientific data review processes.
Professionals in this role will collaborate with clinical teams, biostatisticians, medical writers, regulatory experts, and external partners to ensure high-quality and inspection-ready clinical trial data.
Key Responsibilities
Clinical Data Management Activities
- Oversee data management activities for assigned clinical trials.
- Review requirements for eCRFs and data collection tools.
- Establish data standards, conventions, and quality expectations.
- Define dataset structure and content requirements.
- Monitor timelines and ensure delivery of all data management milestones.
Documentation and Compliance
- Review clinical data management documents and submission packages.
- Ensure documentation quality, accuracy, consistency, and regulatory compliance.
- Maintain real-time inspection readiness for all deliverables.
- Participate in internal and regulatory audits when required.
Trial Management and Collaboration
- Lead interactions with external vendors and CRO partners.
- Collaborate with clinical teams and therapeutic area stakeholders.
- Create and manage key functional plans, including Integrated Review Plans.
- Communicate lessons learned and best practices across projects.
- Participate in process improvement initiatives and system enhancements.
Scientific Data Review
Depending on business requirements, responsibilities may include:
- Management of Study Responsible Scientist (SRS) and Study Responsible Physician (SRP) queries within EDC systems.
- Scientific review of complex study data.
- Coding activities and SAE reconciliation.
- Supporting clinical data review and therapeutic area deliverables.
Eligibility Criteria
Educational Qualifications
Candidates with the following qualifications are eligible:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc (Life Sciences)
- M.Sc (Life Sciences)
- B.Tech Biotechnology
- M.Tech Biotechnology
- B.E/B.Tech (Computer Science)
- Bachelor’s degree in Health Sciences or related disciplines
- Master’s Degree or PhD (Preferred)
Experience Requirements
- Minimum 2 years of experience in Pharmaceutical, CRO, Biotechnology, or related industries.
- Experience in clinical drug development and clinical data management.
- Experience working with cross-functional teams and stakeholders.
- Excellent written and verbal communication skills in English.
Preferred Skills
- Clinical Data Management (CDM)
- Electronic Data Capture (EDC) Systems
- Good Clinical Practice (GCP)
- Clinical Operations
- Data Privacy Standards
- Standard Operating Procedures (SOPs)
- Database Applications
- Biostatistics Knowledge
- Systems Analysis
- Advanced Analytics
- Cross-functional Collaboration
- Report Writing
- Problem Solving and Organization Skills
Why Join Johnson & Johnson?
Johnson & Johnson is a global healthcare innovator dedicated to preventing, treating, and curing complex diseases through cutting-edge pharmaceutical and medical technologies.
Employee Benefits
- Opportunity to work on global clinical trials
- Hybrid work environment
- Exposure to advanced clinical data management technologies
- Career growth within a global healthcare organization
- Cross-functional collaboration with international teams
- Inclusive and diverse workplace culture
- Learning and leadership development opportunities
Estimated Salary
Based on industry benchmarks for Clinical Data Management professionals with 2–5 years of experience:
Estimated Salary Range: ₹9,00,000 – ₹16,00,000 per annum (CTC)
Actual compensation may vary depending on experience, location, and skill set.
How to Apply
