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Alcon Hiring for Clinical Data Management

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Alcon

Bachelorโ€™s degree with clinical research OR Masterโ€™s/PhD in Optometry, Ophthalmology, Vision Science, or related field

Bangalore

2+ years in clinical data management or research operations

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Alcon is hiring for the role of Sr. Associate, Clinical Data Management & Operations in Bangalore, India. This is a high-impact opportunity for candidates with clinical research experience in ophthalmology, optometry, or vision science looking to work in a global R&D environment.

This role focuses on clinical data management, study operations, and scientific analysis, supporting innovative eye care solutions. If you have experience with GCP, CRF design, and clinical data review, this role offers strong career growth in the medical device and clinical research domain.

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๐Ÿ”‘ Key Responsibilities

  • Manage and organize clinical data and study records ensuring accuracy and compliance
  • Support clinical study planning, execution, and reporting
  • Review clinical protocols, statistical analysis plans, and study reports
  • Assist in CRF (Case Report Form) design and data capture tools
  • Perform data entry, source-to-CRF verification, and data quality checks
  • Analyze scientific and clinical data from studies and literature
  • Prepare scientific presentations, literature reviews, and slide decks
  • Compile competitive intelligence (CI) from conferences and journals
  • Coordinate with investigators for:
    • CTRI registrations
    • IRB submissions
    • Study agreements
  • Monitor study progress, compliance, and milestones
  • Handle clinical trial logistics and ancillary supplies management
  • Ensure adherence to GxP, SOPs, and regulatory standards

๐ŸŽ“ Qualifications & Eligibility

Education:

  • Bachelorโ€™s degree with clinical research experience OR
  • Masterโ€™s/PhD in Optometry, Ophthalmology, Vision Science, or related field

Experience:

  • Minimum 2+ years in clinical data management or research operations
  • Experience in clinical study documentation and reporting
  • Exposure to ophthalmology or vision science research preferred

Technical Skills:

  • Strong knowledge of GCP and clinical research regulations
  • Experience with:
    • CRF design
    • Data validation & quality checks
    • Basic biostatistics
  • Proficiency in Excel, PowerPoint, and scientific documentation
  • Data visualization (graphs, tables, dashboards)

๐Ÿ’ผ Key Skills

  • Clinical Data Management
  • Clinical Research Operations
  • Scientific Writing & Literature Review
  • Data Analysis & Visualization
  • Regulatory Compliance (GCP, ISO)
  • Communication & Cross-functional Collaboration

๐Ÿ’ฐ Salary & Benefits

  • Estimated Salary: โ‚น6 LPA โ€“ โ‚น10 LPA (based on experience)
  • Relocation assistance provided
  • Exposure to global R&D projects
  • Opportunity to publish scientific work
  • Work timing: 1 PM โ€“ 10 PM IST

๐Ÿ“ Job Location

  • Bangalore, India

๐Ÿš€ Why Join Alcon?

  • Global leader in eye care and medical devices
  • Strong focus on innovation and patient outcomes
  • Opportunity to work on cutting-edge clinical research
  • Career growth in clinical data management & operations

๐Ÿ“„ How to Apply

Application Link

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