Regulatory Affairs Director – Regenerative Medicine

IQVIA LLC; Washington (District of Columbia); On-site; USD 135,300 - 376,800; Full time

Job summary

IQVIA LLC in Washington, DC is seeking a Director of Regulatory Affairs to manage the regulatory strategy and submissions for client projects. The successful candidate will develop regulatory submissions and communicate effectively with regulatory bodies and clients.

Applicants should have a Bachelor's degree in a scientific field, at least five years of experience in regulatory affairs, and strong project management skills. This role offers a competitive salary and the chance to work within a leading CRO.

Qualifications

• Minimum five years of experience in Regulatory Affairs.
• Experience with FDA oversight of medical products.
• Strong written and verbal communication skills.

Responsibilities

• Manage regulatory submissions for diverse projects.
• Oversee regulatory staff and client relationship management.
• Develop regulatory strategies and ensure project timelines.

Skills

FDA regulations knowledge

Project management

Regulatory submissions expertise

Attention to detail

Analytical skills

Education

Bachelor's degree in a scientific field

MS or PhD preferred

Tools

MS Office

Excel

Job description

IQVIA LLC in Washington, DC is seeking a Director of Regulatory Affairs to manage the regulatory strategy and submissions for client projects. The successful candidate will develop regulatory submissions and communicate effectively with regulatory bodies and clients.

Applicants should have a Bachelor's degree in a scientific field, at least five years of experience in regulatory affairs, and strong project management skills. This role offers a competitive salary and the chance to work within a leading CRO.