Senior Medical Writer

Senior Associate I Medical Writer

• Knowledge of safety guidelines and regulations for medical devices and/or pharmaceutical development and post-market surveillance
• Familiarity with medical terminology and working with large databases.
• Proven ability to analyze, interpret, and discuss safety information relating to multiple therapeutic areas.
• Strong interpersonal, effective communication (written and verbal), and presentation skills.
• Strong organization and time management skills
• Demonstrates attention to detail and accuracy.
• Self-motivated, ability to work under pressure, demonstrating initiative and flexibility.
• High learning agility, ability to work independently and meet targeted timelines in a team-centric environment.
• Experience with (safety or others) issue management

Preferred:

• Knowledge of ophthalmic clinical practice and therapeutic area products

≥ 2 years in medical device and/or pharmaceutical industry (R&D, QA, or Regulatory Affairs)

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Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.

Experience Level

Mid Level