Regulatory Labeling Fellow — Pharma Postdoc

Boehringer Ingelheim; Ridgefield (CT); On-site; USD 60,000 - 80,000; Full time

Job summary

Boehringer Ingelheim is offering a Regulatory Affairs Labeling Content Fellowship based at its U.S. headquarters in Ridgefield, CT.

The program provides pharmacists with exposure to US regulatory labeling and rotations within and beyond Regulatory Affairs to build competencies across therapeutic areas such as cardiology, diabetes, immunology, oncology, and respiratory. As an employee, you will contribute to discovery, development, and delivery of products while gaining insight into a global

Qualifications

• Doctor of Pharmacy degree from ACPE-accredited school or college.
• Strong intrapersonal, active listening, and problem-solving skills.
• Excellent verbal and written communication skills.
• Ability to work independently within provided guidance from team leads.

Responsibilities

• Chair meetings of the Product Label Review Teams (PLRT) for each marketed product. Draft/revise product labeling and compile supportive documentation.
• Coordinate preparation of regulatory labeling documents needed for submissions with other departments.
• Assist with FDA interactions on assigned projects and ensure consistency with CCDS proposals.

Skills

Communication skills

Team collaboration

Problem solving

Education

Doctor of Pharmacy degree (ACPE-accredited)

Tools

Outlook

Word

PowerPoint

Excel

Job description

Boehringer Ingelheim is offering a Regulatory Affairs Labeling Content Fellowship based at its U.S. headquarters in Ridgefield, CT.

The program provides pharmacists with exposure to US regulatory labeling and rotations within and beyond Regulatory Affairs to build competencies across therapeutic areas such as cardiology, diabetes, immunology, oncology, and respiratory. As an employee, you will contribute to discovery, development, and delivery of products while gaining insight into a global