Senior Associate I Medical Writer

Responsibilities

• Analyze, interpret, and discuss safety information relating to multiple therapeutic areas
• Manage medical device and/or pharmaceutical regulatory documentation
• Utilize large databases to support safety monitoring and reporting
• Manage safety-related issues and ensure compliance with regulatory standards
• Maintain high levels of accuracy and attention to detail in all medical writing tasks

Requirements

• Knowledge of safety guidelines and regulations for medical devices and/or pharmaceutical development and post-market surveillance
• Familiarity with medical terminology and experience working with large databases
• Proven ability to analyze and interpret complex safety information
• Strong interpersonal, written, and verbal communication skills
• Experience with safety or other issue management
• Ability to work independently and meet targeted timelines in a team-centric environment

Preferred Qualifications

• Knowledge of ophthalmic clinical practice and therapeutic area products
• At least 2 years of experience in the medical device and/or pharmaceutical industry (R&D, QA, or Regulatory Affairs)

About the Company

Alcon is committed to helping people see better by developing and manufacturing innovative devices to serve the full life cycle of eye care needs. Founded in 1945, Alcon sells products in 180 countries worldwide, ranging from surgical equipment for cataract removal to consumer contact lens solutions.