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Sr. Site Manager

Johnson & Johnson
Johnson & Johnson
5+ years
₹22,00,000 – ₹32,00,000 per yea
Hyderabad, Mumbai, India
10 March 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Site Manager – Clinical Trial Support – Johnson & Johnson (Mumbai / Hyderabad)

Johnson & Johnson is hiring a Senior Site Manager for Clinical Trial Support in Mumbai or Hyderabad, India within its R&D Operations team. In this role, you will act as the primary point of contact between the sponsor and investigational clinical trial sites, ensuring that clinical studies are conducted according to Good Clinical Practice (GCP), regulatory requirements, and company Standard Operating Procedures (SOPs). The position involves overseeing site management activities throughout the clinical trial lifecycle, including site selection, study start-up, monitoring visits, recruitment strategy, and site close-out. You will collaborate with Local Trial Managers, Clinical Trial Assistants, and global study teams to ensure trial quality, data accuracy, and regulatory compliance. This role is ideal for professionals with experience in clinical trial operations, site monitoring, regulatory compliance, and clinical research management within the pharmaceutical or biotechnology industry. The estimated salary for this role ranges from ₹22 LPA to ₹32 LPA depending on experience in clinical trial management and regulatory operations.

Key Responsibilities

  • Serve as the primary contact between the sponsor and clinical trial sites for assigned studies.

  • Support site feasibility assessments and site qualification visits.

  • Manage site initiation, monitoring visits (on-site and remote), and site close-out activities.

  • Ensure compliance with clinical trial protocols, SOPs, GCP guidelines, and regulatory requirements.

  • Coordinate subject recruitment strategies and retention planning with study teams.

  • Ensure proper management of clinical drug supplies, lab kits, and study materials at trial sites.

  • Monitor clinical data entry, query resolution, and overall data quality.

  • Ensure timely reporting of Adverse Events (AE), Serious Adverse Events (SAE), and product quality complaints.

  • Maintain accurate trial documentation, monitoring reports, and regulatory records.

  • Support site audit readiness, CAPA implementation, and regulatory inspections.

  • Mentor junior site managers and contribute to process improvements and training initiatives.

Required Qualifications

  • 3–5 years of experience in clinical trial operations, site management, or clinical research.

  • Strong understanding of Good Clinical Practice (GCP), regulatory guidelines, and clinical trial protocols.

  • Experience with clinical site monitoring, study start-up activities, and clinical data management systems.

  • Strong communication and stakeholder management skills.

  • Ability to work in cross-functional global research teams.

Required Skills

  • Clinical Trial Management

  • Site Monitoring & Site Management

  • GCP / Regulatory Compliance

  • Clinical Data Management

  • Study Start-up & Close-out

  • Risk-Based Monitoring

  • Stakeholder Communication

  • Project & Study Management

Salary

Approximate Salary: ₹22,00,000 – ₹32,00,000 per year (depending on experience in clinical trial operations and site management).