Key Responsibilities:
Write clinical evaluation plans (CEPs), clinical evaluation reports (CERs), and any other relevant documents supporting clinical evaluations.
Ensure the timely production of compliant and high quality documents.
Adhere to the project prioritization, strategies, and timelines.
Communicate project status to supervisor and escalate issues in a timely manner.
Adhere to regulatory requirements and internal policies and processes.
Key Requirements/Minimum Qualifications:
Any Bachelor’s degree/ Health Sciences
2+ years in medical writing
Proficient in Microsoft Office and electronic document management systems
Shift Timings: 12 PM to 9PM with slight flexibility
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.