Non-Clinical Medical Job at Johnson & Johnson, India
Want to work in clinical trials and be the key link between research sites and sponsors? Johnson & Johnson is hiring an Associate Site Manager across major Indian cities. This role is ideal for professionals with experience in clinical trial monitoring and site management. You will play a crucial role in ensuring compliance, data accuracy, and smooth trial execution. The Non-Clinical Medical Job at Johnson & Johnson Careers in India offers hands-on exposure to global clinical research operations. If you are looking to grow in R&D and clinical trials, this is a great opportunity.
About the Company:
Johnson & Johnson is a global leader in healthcare innovation, committed to improving health outcomes worldwide. With expertise across Innovative Medicine and MedTech, the company focuses on developing advanced, patient-centric solutions. Guided by its core values, Johnson & Johnson fosters an inclusive work culture and drives breakthroughs that impact global health.
Job Details:
- Role: Associate Site Manager
- Function: R&D Operations
- Sub Function: Clinical Trial Support
- Category: Analyst (P4 – E24)
- Locations: Mumbai / Bangalore / Hyderabad / Delhi
- Work Pattern: Hybrid
- Job ID: R-064980
- Posted On: May 04, 2026
Key Responsibilities:
- Act as primary contact between sponsor and investigational sites
- Support site feasibility and qualification visits
- Participate in investigator meetings in this Non-Clinical Medical Job at Johnson & Johnson Careers
- Manage site initiation, monitoring (remote/on-site), and close-out activities
- Ensure compliance with protocol, SOPs, GCP, and regulatory guidelines
- Implement risk-based monitoring and resolve site-level issues
- Ensure training of site staff and maintain training records
- Support subject recruitment and retention strategies in this Job in India
- Manage site supplies, clinical drug handling, and documentation
- Ensure timely data entry, query resolution, and data accuracy
- Monitor and report AEs, SAEs, and PQCs within timelines
- Maintain trial documentation and prepare monitoring reports
- Collaborate with Local Trial Manager (LTM) and study teams
- Support audits, CAPA processes, and quality assurance activities
- Track site costs and ensure payments if applicable
- Maintain strong relationships with investigators and stakeholders
- Participate in regulatory submissions (HA, IEC/IRB) where required
- Contribute to process improvements and team training
Educational Requirements for this Job:
- Bachelor’s Degree in Medicine or related field
- MBBS
- PhD (preferred but not mandatory)
Skills Required:
Technical Skills
- Knowledge of clinical trials and operations
- Understanding of GCP and regulatory environment
- Clinical data management and study management
- Research ethics and compliance knowledge
- Laboratory and R&D operations understanding
Core Skills
- Analytical reasoning and problem-solving
- Strong business and communication skills (Business English)
- Time management and execution focus
- Project support and process-oriented approach
- Issue escalation and resolution capability
Preferred Skills
- Experience in clinical trial monitoring (2–4 years)
- Process improvement mindset
- Ability to work in cross-functional teams
Benefits of the Non-Clinical Medical Job:
- Work with a global healthcare leader
- Exposure to international clinical trials and research
- Hybrid work flexibility
- Strong career growth in clinical research and R&D
- Opportunity to collaborate with global teams
- Involvement in innovative healthcare solutions
- Continuous learning and development opportunities
