Are you passionate about medical literature analysis, pharmacovigilance, and regulatory compliance? Alcon, a global leader in eye care innovation, is hiring a Sr. Associate I, Medical Literature Analyst in Bangalore, India. This role offers a unique opportunity to contribute to advancing eye health by conducting literature searches, supporting safety and compliance, and collaborating with international teams.
If you have experience in medical device safety, complaint handling, or pharmacovigilance, this role could be your next big career step.
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Key Responsibilities
As a Medical Literature Analyst at Alcon, you will:
- Develop and execute literature search strategies for CERs, SotA reviews, and Safety/Performance reports.
- Conduct annual literature queries in collaboration with Regulatory Affairs.
- Support Medical Safety, Complaint Intake, and HEOR with evidence-based literature data.
- Summarize publications to identify adverse events, risks, and safety concerns.
- Ensure compliance with SOPs, corporate guidelines, and regulatory standards.
- Collaborate with global teams across time zones to meet project needs.
- Maintain knowledge of ophthalmic terminology, anatomy, and diseases.
- Proactively escalate safety signals, trends, and concerns.
Minimum Qualifications
To be considered, candidates must have:
- Bachelor’s degree in science, pharmacy, healthcare, or related field.
- Experience in Medical Device/Pharma Complaint Handling, Vigilance, or Pharmacovigilance.
- Familiarity with US-based customers and international regulations.
- Strong decision-making, troubleshooting, and communication skills.
- Proficiency in MS Office tools.
- Understanding of medical device safety and post-market vigilance.
Benefits of Joining Alcon
- Work with a world leader in eye health innovation.
- Exposure to global regulatory and clinical operations.
- Career growth opportunities in pharmacovigilance and regulatory research.
- Inclusive and diverse workplace culture.
How to Apply
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