Medical Writer II
Abbott Laboratories•Des Plaines, IL
48d
About The Position
Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions. Incorporate graphs, charts, tables, and statistical analyses from approved source files. Proofread, edit, circulate, assemble, and inspect submission documents for accuracy and compliance. Focus Area: This role is primarily focused on EU IVDR submissions.
Requirements
- 3- 5 years of experience in medical writing or regulatory documentation.
- Strong skills in preparing and editing scientific reports.
- Ability to work with complex data and present it clearly in technical documents
Responsibilities
- Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions.
- Incorporate graphs, charts, tables, and statistical analyses from approved source files.
- Proofread, edit, circulate, assemble, and inspect submission documents for accuracy and compliance.
Benefits
- Medical and Prescription Drug Plans
- Dental Plan
- Vision Plan
- Health Savings Account (for High-Deductible Health Plans)
- Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
- Supplemental Life Insurance
- Short Term Disability (coverage varies by state)
- Long Term Disability
- Critical Illness, Hospital coverage, Accident Insurance
- MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
- 401(k)
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
