Regulatory Affairs Analyst

Highly Competitive Salary
  1. Permanent
  2. Project Manager, Publishing & Submissions, RA Intelligence
  3. United States
North Chicago, USA
Posting date: 02 Jun 2021

Proclinical is currently recruiting for a Regulatory Affairs Analyst with a biopharmaceutical company located in North Chicago, IL.

Job Responsibilities:

  • Reviews, and assess' incoming global regulatory information for entry into registration and documentation management systems.
  • Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.
  • Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects.
  • Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.
  • Participates and contributes to group, department, and cross-functional meetings.
  • May also assist in training junior team members.

Skills and Requirements:

  • Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.
  • Experience/understanding/use of software tools.
  • Demonstrated analytical and communication skills.
  • Skills and knowledge of drug submissions

If you are having difficulty in applying or if you have any questions, please contact Samantha Reader at 267-536-3075.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.